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Peptide clinical trial tracker

Which peptides are actually being tested in people? For each profile, we search ClinicalTrials.gov and keep only studies that name the compound as an intervention. Checked October 8, 2026.

75 of 113 profiles have at least one registered human study; 62 have studies recruiting or active now. A registration is a plan, not a result.

CompoundRecruiting / activeCompletedListed studies
Tirzepatide721082+
Semaglutide662288+
Oxytocin481869+
Leuprolide35843+
Octreotide312969+
Degarelix272865+
Human insulin27937+
Liraglutide243369+
Mazdutide241944
Vasopressin231034+
Triptorelin202044+
Glutathione201033+
Cagrilintide182444
Desmopressin154683+
Teriparatide145184+
Glucagon13115+
Dulaglutide125476+
Thymosin alpha-1121441
Vosoritide12418
Survodutide112536
Retatrutide112235
Cerebrolysin91942
Bivalirudin83674
Enlicitide82634
Calcitonin salmon81531+
HCG81223+
Terlipressin73777+
Linaclotide73551
Abaloparatide71323
Cosyntropin71023
Lanreotide65082+
Pasireotide65075
Exenatide54461+
Ghrelin51829+
Kisspeptin-1051929
Kisspeptin-5451929
Setmelanotide51926
Lixisenatide45364
Teduglutide44148
NAD+415+
Pramlintide34360
Elamipretide31319
Thymosin beta-431119
Tesamorelin3717
Ziconotide3713
Pemvidutide21016
PACAP-382913
MOTS-c203
BPC-157202
GHK-Cu202
L-Carnosine12133
Afamelanotide11823
LL-3711215
VIP11015
Plecanatide11314
Bremelanotide1910
Neuropeptide Y1810
Thymopentin179
Nisotirostide134
Humanin113
Melanotan II102
TB-500101
Enfuvirtide03441
Peptide YY01113
Larazotide0810
TRH (thyrotropin-releasing hormone)057
Orexin-A036
Efpeglenatide015
Argireline034
Nesfatin-1024
MK-677033
ARA-290012
Ipamorelin022
CJC-1295001
Peptide bioregulators (Khavinson peptides)011

Tirzepatide

StudyStatusPhaseStartPeople
Trial of Innovative Fat-loss Focused Approaches in Patients With Class I Obesity: a Comparative Study
NCT07866183 · National Medical Research Center for Therapy and Preventive Medicine
RecruitingNot applicable2026-06-29120
GLP-1 Receptor Agonist Use and Sarcopenia in Obese Individuals Without Diabetes
NCT07858864 · Istanbul Saglik Bilimleri University
Recruiting2026-05-3042
A Master Protocol of Multiple Agents in Adults With Metabolic Dysfunction-Associated Steatotic Liver Disease (SYNERGY-Outcomes)
NCT07165028 · Eli Lilly and Company
RecruitingPhase 32025-10-154500
Mirikizumab and Tirzepatide Administered in Adult Participants With Moderately to Severely Active Crohn's Disease and Obesity or Overweight
NCT06937099 · Eli Lilly and Company
RecruitingPhase 32025-06-26290
A Master Protocol Study (LY900038) of Multiple Intervention-Specific-Appendices (ISAs) in Adult Participants With Obesity or Overweight
NCT06143956 · Eli Lilly and Company
RecruitingPhase 22023-11-171481
Mirikizumab Administered at the Same Time as Tirzepatide in Adult Participants With Moderately to Severely Active Ulcerative Colitis and Obesity or Overweight: Phase 3b Study
NCT06937086 · Eli Lilly and Company
RecruitingPhase 32025-06-26350
A Study of Tirzepatide (LY3298176) on the Reduction on Morbidity and Mortality in Adults With Obesity
NCT05556512 · Eli Lilly and Company
Active, not recruitingPhase 32022-10-1115374
Effectiveness and Safety of Tirzepatide Among Participants With Obesity With or Without Type 2 Diabetes Mellitus (T2DM)
NCT07099742 · Dr. Md. Alimur Reza
Not yet recruiting2026-11364
The Effect of Tirzepatide on Menopausal Vasomotor Symptoms and Biological Aging in Post-menopausal Women With Obesity
NCT07218445 · Mayo Clinic
RecruitingPhase 42026-04-0840
GLP-1s to Enhance Lasting Optimal Weight
NCT06861439 · Wake Forest University Health Sciences
Active, not recruitingPhase 42025-07-0740
Tirzepatide in Obesity-Driven Endometrial Cancer
NCT07065552 · UNC Lineberger Comprehensive Cancer Center
RecruitingEarly phase 12026-04-2720
Tirzepatide in Thrombectomy-Treated Acute Ischemic Stroke: A Randomized Trial
NCT07734792 · yifang zhu
Not yet recruitingPhase 2 / Phase 32026-09-20726
Sequential Therapy Anti-obesitY Medication With Muscle Preservation for Weight Loss and MaintEnance: A PragmAtic Randomized CoNtrolled Trial (STAY-LEAN Trial)
NCT06854614 · The Cleveland Clinic
Active, not recruitingPhase 42025-03-01150
Effects of Tirzepatide on Gut Microbiota and Gastrointestinal Function After Drug Withdrawal in Obese Patients
NCT07847515 · Nanjing First Hospital, Nanjing Medical University
Not yet recruiting2027-02-0180
A Phase 2a Study of ALN-PNP With and Without a GLP1R Agonist in Adult Patients With Homozygous PNPLA3-Related MASLD
NCT07527910 · Regeneron Pharmaceuticals
RecruitingPhase 22026-05-22204

Semaglutide

StudyStatusPhaseStartPeople
Probiotics in Obese Patients Treated With Semaglutide
NCT07847593 · Nordic Biotic Sp. z o.o.
CompletedNot applicable2025-07-09102
GLP-1 Receptor Agonist Use and Sarcopenia in Obese Individuals Without Diabetes
NCT07858864 · Istanbul Saglik Bilimleri University
Recruiting2026-05-3042
Maridebart Cafraglutide Versus Semaglutide in Participants With Type 2 Diabetes
NCT07866066 · Amgen
Not yet recruitingPhase 32026-11-021300
A Research Study on How Well Semaglutide Helps Children and Teenagers With Excess Body Weight Lose Weight
NCT05726227 · Novo Nordisk A/S
Active, not recruitingPhase 32023-07-07212
A Research Study to Look at How Semaglutide Compared to Placebo Affects Diabetic Eye Disease in People With Type 2 Diabetes
NCT03811561 · Novo Nordisk A/S
Active, not recruitingPhase 32019-05-081500
Visceral Adipose Tissue and Liver Changes Associated With Semaglutide in CKD
NCT07187830 · University of Alberta
Recruiting2026-02-2352
A Research Study Comparing How Well Different Doses of the Medicine UBT251 Lower Blood Sugar in People With Type 2 Diabetes
NCT07668388 · Novo Nordisk A/S
RecruitingPhase 22026-06-22300
Semaglutide in Women With Polycystic Ovary Syndrome and Obesity
NCT06896981 · Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh
CompletedPhase 2 / Phase 32025-01-0131
Imaging in Semaglutide Study
NCT07695454 · The Cleveland Clinic
Recruiting2026-07-3010
A Study to Evaluate the Effect of Retatrutide on Insulin Secretion and Insulin Sensitivity in Adult Participants With Type 2 Diabetes Mellitus
NCT06982859 · Eli Lilly and Company
Active, not recruitingPhase 12025-06-0295
Efficacy and Safety of Ribupatide Administered Once Weekly Compared With Semaglutide and Placebo in Participants Living With Obesity Who Do Not Have Diabetes
NCT07284979 · Kailera
Active, not recruitingPhase 32025-12-301270
Tapered Versus Abrupt Discontinuation of Semaglutide After Treatment of Recurrent Weight Gain or Suboptimal Response Following Metabolic and Bariatric Surgery
NCT07859176 · General Committee of Teaching Hospitals and Institutes, Egypt
Not yet recruitingPhase 42026-10100
Semaglutide Given Before and After Conversion of Sleeve Gastrectomy to Roux-en-Y Gastric Bypass for Recurrent Weight Gain
NCT07859163 · General Committee of Teaching Hospitals and Institutes, Egypt
Not yet recruitingPhase 42026-10100
Immediate Versus Criterion-triggered Semaglutide for Suboptimal Clinical Response One Year After Primary Metabolic and Bariatric Surgery
NCT07859189 · General Committee of Teaching Hospitals and Institutes, Egypt
Not yet recruitingPhase 42026-10100
Semaglutide 2.4 mg Once Weekly for Recurrent Weight Gain After Metabolic and Bariatric Surgery (RESURGE)
NCT07859150 · General Committee of Teaching Hospitals and Institutes, Egypt
Not yet recruitingPhase 42026-10104

Oxytocin

StudyStatusPhaseStartPeople
Intranasal Oxytocin for Methamphetamine Withdrawal in Women
NCT05760807 · Turning Point
CompletedNot applicable2023-03-2910
Effect of Intravenous Oxytocin on Post Dural Puncture Headache After Caesarean Sections
NCT07853924 · Assiut University
Not yet recruitingPhase 42026-09100
Effects of Intranasal Oxytocin in the Treatment of Benzodiazepine Withdrawal: A Pilot RCT
NCT06757517 · St. Olavs Hospital
CompletedPhase 22022-03-0166
Use of Intranasal Oxytocin During Detoxification of Crack Cocaine
NCT04306354 · Pontificia Universidade Católica do Rio Grande do Sul
CompletedPhase 1 / Phase 22018-09-1784
Efficacy of Intravenous Oxytocin to Speed Recovery After THA
NCT07430228 · Wake Forest University Health Sciences
Enrolling by invitationPhase 22026-1080
Oromucosal Oxytocin and Vasopressin Modulation of Emotional Face Attention
NCT07838493 · University of Electronic Science and Technology of China
RecruitingNot applicable2026-09-18120
The Effects of Oxytocin on Fairness Perception and Related Prosocial Behaviors
NCT07815496 · University of Electronic Science and Technology of China
RecruitingNot applicable2026-09-0580
Mother-Baby Study - Observational
NCT06039878 · University of Michigan
Active, not recruitingNot applicable2023-12-21250
Induction of Labor After Cesarean Using Foley Alone vs. Concurrent Foley and Oxytocin
NCT07006896 · University of Pennsylvania
Active, not recruitingNot applicable2025-07-10100
Generate and Test the Reliability of a PD Model of OXT on Pupillary Hippus as a Measure of CNS Activity
NCT04427709 · Wake Forest University Health Sciences
TerminatedPhase 22020-11-304
The Effect of Simulation-Based Oxytocin Induction Training on Midwifery Students' Knowledge and Anxiety Levels
NCT07788495 · Melisa Gündeş
CompletedNot applicable2024-11-1180
Effect of Oxytocin Bolus Versus Slow Infusion on Haemodynamic Stability During Caesarean Section Under Spinal Anaesthesia
NCT07784478 · Khyber Girls Medical College
Not yet recruitingNot applicable2026-09-0160
Oxytocin in Postmenopausal Women
NCT07742124 · University Hospital, Basel, Switzerland
Recruiting2026-08-2030
Identifying Oxytocin Deficiency in Pediatric Patients With Pituitary Disease
NCT07568509 · Massachusetts General Hospital
RecruitingEarly phase 12026-08-1720
Oxytocin-Augmented Group Psychotherapy for Patients With Schizophrenia - an Oxytocin-dose Comparison
NCT07265180 · Charite University, Berlin, Germany
RecruitingNot applicable2025-09-08120

Leuprolide

StudyStatusPhaseStartPeople
Standard Systemic Therapy With or Without Definitive Treatment in Treating Participants With Metastatic Prostate Cancer
NCT03678025 · SWOG Cancer Research Network
RecruitingPhase 32018-09-241273
Neoadjuvant ADT + Darolutamide With Pembrolizumab, Followed by Adjuvant Pembrolizumab in Molecularly Stratified High-Risk Prostate Cancer
NCT07027124 · Icahn School of Medicine at Mount Sinai
RecruitingPhase 22026-05-2140
Phase IIIb Study of Ribociclib + ET in Early Breast Cancer
NCT05827081 · Novartis Pharmaceuticals
RecruitingPhase 32024-02-281400
A Single-Arm Phase II Study of Neoadjuvant Intensified Androgen Deprivation (Leuprolide and Abiraterone Acetate) in Combination With AKT Inhibition (Capivasertib) for High-Risk Localized Prostate Cancer With PTEN Loss
NCT05593497 · VA Office of Research and Development
RecruitingPhase 22024-05-3130
Ovarian Suppression Evaluating Subcutaneous Leuprolide Acetate in Breast Cancer
NCT04906395 · Tolmar Inc.
Active, not recruitingPhase 32021-07-01250
The LUCINDA Trial: LeUprolide Plus Cholinesterase Inhibition to Reduce Neurological Decline in Alzheimer's
NCT03649724 · Weill Medical College of Cornell University
CompletedPhase 22020-11-2786
Study of PSMA-targeted Therapy and Androgen Receptor Suppression in Low-volume Metastatic ProstatE Cancer: SPARKLE Trial
NCT07650240 · Mayo Clinic
RecruitingPhase 22026-08-04202
Antiandrogen Therapy and Radiation Therapy With or Without Docetaxel in Treating Patients With Prostate Cancer That Has Been Removed by Surgery
NCT03070886 · NRG Oncology
Active, not recruitingPhase 2 / Phase 32017-04-05612
A Study for Subjects With Prostate Cancer Who Previously Participated in an Enzalutamide Clinical Study
NCT02960022 · Astellas Pharma Global Development, Inc.
Active, not recruitingPhase 22016-12-22900
Neoadjuvant Endocrine Therapy Combined With Chemotherapy in ER-positive, HER2-negative Stage I-III Breast Cancer
NCT07801898 · The Second Hospital of Anhui Medical University
Not yet recruitingPhase 22026-09-3036
Treating Prostate Cancer That Has Come Back After Surgery With Apalutamide and Targeted Radiation Based on PET Imaging
NCT04423211 · ECOG-ACRIN Cancer Research Group
RecruitingPhase 32020-10-08804
Two Studies for Patients With Unfavorable Intermediate Risk Prostate Cancer Testing Less Intense Treatment for Patients With a Low Gene Risk Score and Testing a More Intense Treatment for Patients With a Higher Gene Risk Score, The Guidance Trial
NCT05050084 · NRG Oncology
Active, not recruitingPhase 32021-12-062050
Two Studies for Patients With High Risk Prostate Cancer Testing Less Intense Treatment for Patients With a Low Gene Risk Score and Testing a More Intense Treatment for Patients With a High Gene Risk Score, The PREDICT-RT Trial
NCT04513717 · NRG Oncology
Active, not recruitingPhase 32021-01-212753
Finite Androgen Ablation With or Without Abiraterone Acetate and Prednisone in Treating Patients With Recurrent Prostate Cancer
NCT01786265 · M.D. Anderson Cancer Center
Active, not recruitingPhase 22013-02-05310
Bipolar Androgen Therapy to Restore Sensitivity to Androgen Deprivation Therapy for Patients With Metastatic Castration Resistant Prostate Cancer
NCT06305598 · Roswell Park Cancer Institute
Active, not recruitingPhase 12024-12-193

Octreotide

StudyStatusPhaseStartPeople
Study of RYZ101 Compared With SOC in Pts w Inoperable SSTR+ Well-differentiated GEP-NET That Has Progressed Following 177Lu-SSA Therapy
NCT05477576 · RayzeBio, Inc.
Active, not recruitingPhase 32022-03-24343
Prospective Evaluation of 68Ga-DOTATATE PET/CT, Octreotide and F-DOPA PET Imaging in Ectopic Cushing Syndrome
NCT02019706 · National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
RecruitingPhase 22014-02-1280
Octreotide Acetate and Recombinant Interferon Alfa-2b or Bevacizumab in Treating Patients With Metastatic or Locally Advanced, High-Risk Neuroendocrine Tumor
NCT00569127 · National Cancer Institute (NCI)
Active, not recruitingPhase 32007-12-01427
An Observational Study of Octreotide Subcutaneous Depot in Patients With Acromegaly
NCT07583563 · Camurus AB
Recruiting2026-06-05200
A Phase 1 Study to Evaluate the Relative Bioavailability of Octreotide Acetate Tablets(T25) Compared to MYCAPSSA® and The Food Effect on Pharmacokinetics Of Octreotide Acetate Tablets(T25)
NCT07663318 · Triastek (Shanghai) Limited
CompletedPhase 12026-06-2518
Randomized Interval Assessment Trial of Lu177-Dotatate in Slowly Progressive G1-2 Advanced Midgut Neuroendocrine Tumors
NCT06878664 · Grupo Espanol de Tumores Neuroendocrinos
RecruitingPhase 32025-06-12166
A Clinical Trial to Evaluate Safety, Efficacy, Pharmacokinetics, and Pharmacodynamics of Octreotide Long-acting Injection in Patients With Acromegaly
NCT07814651 · CSPC ZhongQi Pharmaceutical Technology Co., Ltd.
CompletedPhase 22024-04-1678
Study to Evaluate the Efficacy and Safety of [177Lu]Lu-DOTA-TATE in Patients With Grade 1 and Grade 2 Advanced GEP-NET
NCT06784752 · Novartis Pharmaceuticals
RecruitingPhase 32025-05-30240
Graded Insulin Suppression Test P&F
NCT06592261 · Columbia University
RecruitingPhase 12024-09-1615
A Trial to Assess Efficacy and Safety of Octreotide Subcutaneous Depot in Patients With Acromegaly
NCT04076462 · Camurus AB
CompletedPhase 32019-08-1972
A Trial to Assess Efficacy and Safety of Octreotide Subcutaneous Depot in Patients With GEP-NET
NCT05050942 · Camurus AB
Active, not recruitingPhase 32021-10-22332
RAD001 Plus Octreotide Depot in Metastatic or Unresectable Low Grade Neuroendocrine Carcinoma
NCT00113360 · M.D. Anderson Cancer Center
CompletedPhase 22005-0167
A Phase III Clinical Trial to Evaluate the Efficacy and Safety of Octreotide Long-acting Injection in Patients With Acromegaly
NCT07623824 · CSPC ZhongQi Pharmaceutical Technology Co., Ltd.
Not yet recruitingPhase 32026-05-31154
A Trial to Assess the Efficacy and Safety of Octreotide Subcutaneous Depot in Patients With PLD
NCT05281328 · Camurus AB
Active, not recruitingPhase 2 / Phase 32022-06-2871
An Open-label Phase 3 Study of Lutetium (177Lu) Oxodotreotide Injection in Subjects With Advanced Gastrointestinal Pancreatic Neuroendocrine Tumors.
NCT05884255 · Jiangsu HengRui Medicine Co., Ltd.
RecruitingPhase 32023-07-06220

Degarelix

StudyStatusPhaseStartPeople
Standard Systemic Therapy With or Without Definitive Treatment in Treating Participants With Metastatic Prostate Cancer
NCT03678025 · SWOG Cancer Research Network
RecruitingPhase 32018-09-241273
A Study of BMS986365 in Combination With Degarelix in People With Prostate Cancer
NCT07335796 · Memorial Sloan Kettering Cancer Center
Active, not recruitingPhase 22026-01-097
Efficacy Study of Switching to a Lutenizing Hormone-releasing Hormone (LHRH) Antagonist From a LHRH Agonist to Treat Progressive Castrate Resistant Prostate Cancer (CRPC)
NCT01630967 · British Columbia Cancer Agency
WithdrawnPhase 22012-080
Androgen Deprivation, With or Without pTVG-AR, and With or Without T-Cell Checkpoint Blockade, in Patients With Newly Diagnosed, High-Risk Prostate Cancer
NCT04989946 · University of Wisconsin, Madison
Active, not recruitingPhase 1 / Phase 22021-12-1657
Antiandrogen Therapy and Radiation Therapy With or Without Docetaxel in Treating Patients With Prostate Cancer That Has Been Removed by Surgery
NCT03070886 · NRG Oncology
Active, not recruitingPhase 2 / Phase 32017-04-05612
TRial on the Endocrine Activity of Neoadjuvant Degarelix
NCT02005887 · ETOP IBCSG Partners Foundation
CompletedPhase 22014-0251
ETHAN - ET for Male BC
NCT05501704 · Jose Pablo Leone
RecruitingPhase 22023-10-1160
Treating Prostate Cancer That Has Come Back After Surgery With Apalutamide and Targeted Radiation Based on PET Imaging
NCT04423211 · ECOG-ACRIN Cancer Research Group
RecruitingPhase 32020-10-08804
Two Studies for Patients With Unfavorable Intermediate Risk Prostate Cancer Testing Less Intense Treatment for Patients With a Low Gene Risk Score and Testing a More Intense Treatment for Patients With a Higher Gene Risk Score, The Guidance Trial
NCT05050084 · NRG Oncology
Active, not recruitingPhase 32021-12-062050
Two Studies for Patients With High Risk Prostate Cancer Testing Less Intense Treatment for Patients With a Low Gene Risk Score and Testing a More Intense Treatment for Patients With a High Gene Risk Score, The PREDICT-RT Trial
NCT04513717 · NRG Oncology
Active, not recruitingPhase 32021-01-212753
Finite Androgen Ablation With or Without Abiraterone Acetate and Prednisone in Treating Patients With Recurrent Prostate Cancer
NCT01786265 · M.D. Anderson Cancer Center
Active, not recruitingPhase 22013-02-05310
Assessing Efficacy of Neoadjuvant ADT in Localized High-Risk Prostate Cancer Patients Utilizing 18F-Flotufolastat PSMA PET/CT
NCT07455903 · Baptist Health South Florida
RecruitingPhase 22026-07-2950
Androgen Deprivation Therapy Prior to Prostatectomy for Patients With Intermediate and High Risk Prostate Cancer
NCT01542021 · Memorial Sloan Kettering Cancer Center
CompletedNot applicable2012-02-2441
Stereotactic Body Radiation Therapy Plus Immediate or Delayed Androgen Receptor Pathway Inhibitor and Androgen Deprivation Therapy or Salvage Radiation Therapy for the Treatment of Prostate Cancer, DIVINE Trial
NCT06378866 · Mayo Clinic
RecruitingPhase 22024-06-03532
NeoAdjuvant Theranostic Lutetium Study: The Nautilus Trial
NCT06066437 · M.D. Anderson Cancer Center
RecruitingPhase 1 / Phase 22024-03-296

Human insulin

StudyStatusPhaseStartPeople
Supporting Medtronic 780G Insulin Pump Adoption in Latino Patients: A Spanish - Language Training Initiative
NCT07720388 · University of Colorado, Denver
RecruitingNot applicable2026-10-0215
Enhancing the Anabolic Effect of Perioperative Nutrition With Insulin While Maintaining Normoglycemia
NCT02032953 · McGill University Health Centre/Research Institute of the McGill University Health Centre
WithdrawnPhase 42013-120
Clinical Trial for the Study of Stress and Exercise Impact on Glucose Levels and Additional Physiological Signals. Stress, Insulin and Exercise Study: a Trial in Argentina
NCT07865923 · National Council of Scientific and Technical Research, Argentina
CompletedNot applicable2024-03-055
The Role of Endocannabinoids in Insulin Production and Action
NCT01517100 · National Institute on Aging (NIA)
CompletedPhase 12012-01-0545
The Real-World Control-IQ Glycemic Control and Quality of Life Study in Type 1 Diabetes in France
NCT07211126 · Tandem Diabetes Care, Inc.
Recruiting2026-03-03350
Genetic Studies of Insulin and Diabetes
NCT00001987 · National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Recruiting1976-02-011200
Think-Find-Solve Activities for Insulin Self-Management in Type 1 Diabetes
NCT07670572 · Marmara University
RecruitingNot applicable2026-10-0540
To Study the Efficacy and Safety of Medtronic 780G Insulin Pump in People With Gastroparesis and Type 1 Diabetes.
NCT07287943 · Viral N. Shah
RecruitingNot applicable2026-02-0934
Insulin and Insulin Pulses During Fasting
NCT06424015 · Mayo Clinic
RecruitingNot applicable2024-09-1560
SNIFF - Combo INI+EMPA Trial
NCT05081219 · Wake Forest University Health Sciences
CompletedPhase 22021-09-1447
Effect of Probiotics Versus Metformin on Glycemic Control, Insulin Sensitivity and Insulin Secretion in Prediabetes.
NCT04341571 · University of Guadalajara
Active, not recruitingPhase 22019-10-2430
DECIDE: A Comparative Effectiveness Trial of Metformin Versus Insulin for the Treatment of Gestational Diabetes
NCT06445946 · Ohio State University
RecruitingPhase 42024-08-011572
RESET-INSPIRE Study: Insulin Sensitivity & Population Intervention With Real-time Evaluation Using CGM
NCT07861191 · National University Health System, Singapore
Recruiting2026-07-27270
A Study to Evaluate the Effect of Retatrutide on Insulin Secretion and Insulin Sensitivity in Adult Participants With Type 2 Diabetes Mellitus
NCT06982859 · Eli Lilly and Company
Active, not recruitingPhase 12025-06-0295
A Study of LY3938577 in Healthy Participants and Participants With Type 1 Diabetes Mellitus (T1DM)
NCT06280703 · Eli Lilly and Company
CompletedPhase 12024-05-15121

Liraglutide

StudyStatusPhaseStartPeople
The Evira Study: Additional Support During Obesity Treatment
NCT06836284 · Karolinska Institutet
RecruitingNot applicable2026-02-1340
Effect of Liraglutide in Obese Women With Polycystic Ovary Syndrome
NCT05965908 · Beni-Suef University
CompletedPhase 32024-08-01183
Effect of Exercise and/or Liraglutide on Vascular Dysfunction and Insulin Sensitivity in Type 2 Diabetes ( ZQL007)
NCT03883412 · University of Virginia
RecruitingPhase 42019-02-2860
LIGHT-MCI Trial: GLP-1 Agonist, SGLT2 Inhibitor, and DPP-4 Inhibitor for MCI Remission in Type 2 Diabetes
NCT05313529 · The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School
CompletedNot applicable2022-10-08396
Examination of How the Duration of Fasting and Temporary Stopping of GLP-1 Medications Affect the Amount of Food Left in the Stomach in People Using Liraglutide (Injected), Semaglutide (Taken by Mouth) or Semaglutide (Injected)
NCT07225816 · Novo Nordisk A/S
RecruitingPhase 12025-11-0771
SCALE KIDS: Research Study to Look at How Well a New Medicine is at Lowering Weight in Children With Obesity
NCT04775082 · Novo Nordisk A/S
Active, not recruitingPhase 32021-03-0478
Use of Liraglutide in Children Aged 6 to 12 Years With Severe Obesity
NCT07590219 · University of Sao Paulo General Hospital
Active, not recruitingPhase 42024-03-3030
Effects of Exercise and GLP-1 Agonism on Muscle Microvascular Perfusion and Insulin Action in Adults With Metabolic Syndrome
NCT04575844 · University of Virginia
RecruitingPhase 42020-11-0180
Saxenda: Underlying Mechanisms and Clinical Outcomes
NCT02944500 · Beth Israel Deaconess Medical Center
Active, not recruitingPhase 42016-1128
Liraglutide Effect in Atrial Fibrillation
NCT03856632 · University of Miami
Active, not recruitingPhase 42019-03-1860
Timely Detection of Treatment Emergent Serious and Non-serious Adverse Events for Saxenda® in Mexican Patients
NCT02773355 · Novo Nordisk A/S
Completed2016-05-1627
Study of Liraglutide (A Weight Loss Drug) in High Risk Obese Participants With Cognitive and Memory Issues
NCT06171152 · University of Chicago
SuspendedEarly phase 12024-01-2630
RWS of of Liraglutide Alone and in Combination With Orlistat for Weight Loss in Overweight/Obese Patients.
NCT07301437 · The Fourth Affiliated Hospital of Zhejiang University School of Medicine
Not yet recruitingPhase 42026-05-01120
Effects of GH and Lirglutide on AgRP
NCT05681299 · Columbia University
RecruitingPhase 42023-05-0140
Pharmacological Treatment - An Overview of Its Role in Managing Childhood Obesity
NCT07304141 · Göteborg University
Completed2023-12-20128

Mazdutide

StudyStatusPhaseStartPeople
A Master Protocol Study (LY900038) of Multiple Intervention-Specific-Appendices (ISAs) in Adult Participants With Obesity or Overweight
NCT06143956 · Eli Lilly and Company
RecruitingPhase 22023-11-171481
A Study of HRS-4729 Injection in Participants With Type 2 Diabetes
NCT07843862 · Fujian Shengdi Pharmaceutical Co., Ltd.
Not yet recruitingPhase 22026-10240
Pre-hepatectomy Rehabilitation in Obese MASLD-Complicated Living Liver Donors With Mazdutide (PRIME)
NCT07718126 · West China Hospital
RecruitingPhase 42026-09-0160
A Study of IBI362 in Subjects With HFpEF or HFmrEF Combined With Obesity
NCT06862908 · Innovent Biologics (Suzhou) Co. Ltd.
Active, not recruitingPhase 22025-03-26141
Efficacy of Mazdutide on Fatty Pancreas
NCT07803705 · Tongji Hospital
Not yet recruitingNot applicable2026-11-15194
Efficacy of Mazdutide for Treating PCOS
NCT06519656 · Shanghai Zhongshan Hospital
CompletedPhase 1 / Phase 22024-10-2143
Mazdutide for Weight Management and Gout in Adults With Obesity
NCT07824895 · Hongwei Jiang
Not yet recruitingPhase 42026-09-1530
ASCEND-1: Lifestyle Intervention Plus Mazdutide for Weight Management
NCT07517042 · Shanghai Zhongshan Hospital
RecruitingNot applicable2026-06-10420
Mazdutide in Type 2 Diabetes With Early-Stage Cognitive Impairment (LIGHT-COG Study)
NCT07083154 · The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School
RecruitingPhase 32025-09-27420
Body-weight Reduction Effect on Portal Hypertension in Compensated Cirrhosis
NCT07797101 · The Second Affiliated Hospital of Chongqing Medical University
Not yet recruitingNot applicable2026-09-0150
Effect of Mazdutide on Coronary Plaque in Patients With Coronary Atherosclerosis and Overweight or Obesity
NCT07657676 · China National Center for Cardiovascular Diseases
Not yet recruitingPhase 42026-09-01116
Mazdutide Plus LNG-IUS for Fertility-Sparing Treatment of AEH or Early Endometrial Cancer
NCT07781150 · Tongji Hospital
Not yet recruitingPhase 22026-11-01128
QUARTET-DKD: Quadruple Therapy for Type 2 Diabetic Nephropathy
NCT07775846 · Huijie Zhang
Not yet recruitingPhase 42026-09-01820
Mazdutide for Remission of Type 2 Diabetes: Multicentre, Double Blind, Randomised, Placebo Controlled Trial
NCT07767552 · Yanbing Li
Not yet recruitingNot applicable2026-09-30249
Efficacy and Safety of Mazdutide in Patients With Type 2 Diabetes Mellitus and Moderate to Severe Nonalcoholic Fatty Liver Disease Previously Treated With Semaglutide
NCT07713992 · Tianjin Medical University
Not yet recruitingNot applicable2026-09-1572

Vasopressin

StudyStatusPhaseStartPeople
Intracervical Vasopressin
NCT07102615 · Prisma Health-Upstate
RecruitingPhase 42025-10-3050
CAlcium and VAsopressin Following Injury Early Resuscitation (CAVALIER) Trial
NCT05958342 · Jason Sperry
RecruitingPhase 22024-06-301050
Oromucosal Oxytocin and Vasopressin Modulation of Emotional Face Attention
NCT07838493 · University of Electronic Science and Technology of China
RecruitingNot applicable2026-09-18120
Hemodynamic Effect of Norepinephrine Versus Vasopressin on the Pulmonary Circulation in Cardiac Surgery Patients:
NCT04501861 · The Cleveland Clinic
CompletedPhase 32020-11-05164
Early Versus Late Adjunctive Vasopressin in Septic Shock
NCT06709573 · The Cleveland Clinic
RecruitingPhase 42025-04-29300
Vasopressin for Septic Shock Pragmatic Trial
NCT06217562 · Intermountain Health Care, Inc.
CompletedPhase 42024-02-013959
Effects of Intranasal Oxytocin in Patients With Arginine-vasopressin Deficiency
NCT04789148 · Elizabeth Austen Lawson
RecruitingPhase 12025-09-1040
Effect of Adding Vasopressin on Cardiac Output, Blood Pressure, Diuresis, and Tissue Perfusion Indices in Patients With Septic Shock
NCT07697144 · Assistance Publique - Hôpitaux de Paris
Not yet recruiting2026-08-01200
Vasopressin and Pain Perception in the Brain
NCT03446456 · University of Maryland, Baltimore
RecruitingPhase 1 / Phase 22018-09-1756
Vasopressin and Epinephrine Versus Epinephrine Alone in Cardiac Arrest
NCT00127907 · Hospices Civils de Lyon
CompletedPhase 42004-05-022416
Intranasal Vasopressin Treatment in Children With Autism
NCT03204786 · Stanford University
CompletedPhase 2 / Phase 32018-02-20157
Effect of Vasopressin Versus Norepinephrine on Post-operative Mean Pulmonary Arterial Pressure Following Pulmonary Endarterectomy Surgery,
NCT07614438 · Fondation Hôpital Saint-Joseph
Not yet recruitingPhase 22026-08-0190
Vasopressin in Intraabdominal Pressure Elevation
NCT03707054 · The Cleveland Clinic
CompletedNot applicable2017-04-2816
Vasopressin vs. Epinephrine During Neonatal Cardiopulmonary Resuscitation
NCT05738148 · University of Alberta
Active, not recruitingPhase 12023-11-278
Effects of Ephedrine, Phenylephrine, Norepinephrine and Vasopressin on Contractility of Human Myometrium and Umbilical Vessels: An In-vitro Study
NCT04053478 · Samuel Lunenfeld Research Institute, Mount Sinai Hospital
RecruitingNot applicable2019-07-08144

Triptorelin

StudyStatusPhaseStartPeople
Standard Systemic Therapy With or Without Definitive Treatment in Treating Participants With Metastatic Prostate Cancer
NCT03678025 · SWOG Cancer Research Network
RecruitingPhase 32018-09-241273
Ovulation Trigger Strategies in Low Ovarian Reserve (TRIGGERBEST)
NCT07816562 · Fundación para la Investigación del Hospital Clínico de Valencia
RecruitingPhase 32024-09-17126
Intranasal Nafarelin For Triggering Oocyte Maturation
NCT06763926 · Fundacion Dexeus
Not yet recruitingPhase 42026-10-15154
TRial on the Endocrine Activity of Neoadjuvant Degarelix
NCT02005887 · ETOP IBCSG Partners Foundation
CompletedPhase 22014-0251
Triptorelin for the Prevention of Ovarian Damage in Adolescents and Young Adults With Cancer
NCT06513962 · Children's Oncology Group
RecruitingPhase 32025-02-2760
Suppression of Ovarian Function With Either Tamoxifen or Exemestane Compared With Tamoxifen Alone in Treating Premenopausal Women With Hormone-Responsive Breast Cancer
NCT00066690 · ETOP IBCSG Partners Foundation
CompletedPhase 32003-12-173066
Treating Prostate Cancer That Has Come Back After Surgery With Apalutamide and Targeted Radiation Based on PET Imaging
NCT04423211 · ECOG-ACRIN Cancer Research Group
RecruitingPhase 32020-10-08804
Two Studies for Patients With Unfavorable Intermediate Risk Prostate Cancer Testing Less Intense Treatment for Patients With a Low Gene Risk Score and Testing a More Intense Treatment for Patients With a Higher Gene Risk Score, The Guidance Trial
NCT05050084 · NRG Oncology
Active, not recruitingPhase 32021-12-062050
Two Studies for Patients With High Risk Prostate Cancer Testing Less Intense Treatment for Patients With a Low Gene Risk Score and Testing a More Intense Treatment for Patients With a High Gene Risk Score, The PREDICT-RT Trial
NCT04513717 · NRG Oncology
Active, not recruitingPhase 32021-01-212753
Assessing Efficacy of Neoadjuvant ADT in Localized High-Risk Prostate Cancer Patients Utilizing 18F-Flotufolastat PSMA PET/CT
NCT07455903 · Baptist Health South Florida
RecruitingPhase 22026-07-2950
Testing the Addition of Darolutamide to Hormonal Therapy (Androgen Deprivation Therapy [ADT]) After Surgery for Men With High-Risk Prostate Cancer, The ERADICATE Study
NCT04484818 · ECOG-ACRIN Cancer Research Group
Active, not recruitingPhase 32021-03-0127
Stereotactic Body Radiation Therapy Plus Immediate or Delayed Androgen Receptor Pathway Inhibitor and Androgen Deprivation Therapy or Salvage Radiation Therapy for the Treatment of Prostate Cancer, DIVINE Trial
NCT06378866 · Mayo Clinic
RecruitingPhase 22024-06-03532
Ultra-Long GnRH-a Pretreatment for FET Outcomes in Patients With Deep Infiltrating Endometriosis
NCT07696351 · Li-jun Ding
RecruitingPhase 42025-08-01120
Study of Quality of Life and Hormone Levels in Premenopausal Participants With Early Breast Cancer Receiving Triptorelin Plus Additional Cancer Treatment
NCT05377684 · Ipsen
Completed2022-06-09450
High-Dose Brachytherapy in Treating Patients With Prostate Cancer
NCT02346253 · Stanford University
CompletedNot applicable2015-01-13146

Glutathione

StudyStatusPhaseStartPeople
The Impact of Qualia Gluthathione+ on Blood Glutathione Levels
NCT07221955 · Qualia Life Sciences
CompletedNot applicable2025-11-3056
Adia Med of Winter Park LLC Autism Spectrum Disorder Research Study
NCT07304440 · Adia Med of Winter Park LLC
RecruitingPhase 12026-05-01100
Glutathione, Brain Metabolism and Inflammation in Alzheimer's Disease
NCT04740580 · Baylor College of Medicine
Active, not recruitingEarly phase 12022-02-1552
Glutathione in Mild Cognitive Impairment
NCT03493178 · Baylor College of Medicine
Active, not recruitingEarly phase 12018-04-1960
Clinical Study to Assess Safety, Efficacy and In-Use Tolerability of Oziva Bioactive Gluta Fizzy Effervescent Tablets on Subjects With Facial Dark Spots Such as Pimple Marks, Sunspots, Age Spots and Uneven Skin Tone
NCT07162623 · NovoBliss Research Pvt Ltd
CompletedNot applicable2025-09-0262
Comparison of Gingival Depigmentation Using Microneedling and Microneedling With Glutathione Gel - A Split Mouth Clinical Trial
NCT07748507 · Krishnadevaraya College of Dental Sciences & Hospital
CompletedNot applicable2025-06-2515
Intranasal Insulin and Glutathione as an Add-On Therapy in Parkinson's Disease
NCT05266417 · Gateway Institute for Brain Research
RecruitingPhase 22022-02-0756
S-Acetyl Glutathione and Performance Recovery in Soccer
NCT07690124 · University of Thessaly
Not yet recruitingNot applicable2026-09-0120
Adia Med of Winter Park LLC Chronic Kidney Disease Research Study
NCT07572890 · Adia Med of Winter Park LLC
RecruitingPhase 12026-05-18100
GAIP ASD Research Study
NCT07622316 · Greater Atlanta Integrative Pediatrics
RecruitingPhase 12026-06-01100
Gingival Hyperpigmentation Treatment
NCT07595705 · Cairo University
RecruitingPhase 22025-08-0130
Enrichment of Glutathione Using Gamma-glutamylcysteine Supplementation in Parkinson's Disease Patients.
NCT07064005 · Pravat Mandal
RecruitingPhase 12026-03-2312
Evaluation of the Efficacy of Oral Tranexamic Acid and Glutathione-assisted Microneedling in Treatment of Melasma
NCT07448415 · Assiut University
Not yet recruitingPhase 2 / Phase 32026-0242
Pharmacokinetics and Safety of a New Micellar Glutathione Formulation
NCT06345950 · Factors Group of Nutritional Companies Inc.
CompletedNot applicable2022-06-2116
Investigating the Effect of Diroximel Fumarate on Glutathione in Schizophrenia
NCT06957808 · King's College London
RecruitingNot applicable2025-01-1030

Cagrilintide

StudyStatusPhaseStartPeople
Weight Loss in People Living With Overweight or Obesity and Type 2 Diabetes Following Treatment With Cagrilintide
NCT07220759 · Novo Nordisk A/S
Active, not recruitingPhase 32025-11-05330
Research Study on How People With Type 2 Diabetes Tolerate Switching From Semaglutide to Cagrisema
NCT07817251 · Novo Nordisk A/S
RecruitingPhase 32026-09-16210
A Research Study to Look at How Two Different Doses of CagriSema and One Dose of Semaglutide Help People Living With Obesity With or Without Type 2 Diabetes Lose Weight
NCT07564414 · Novo Nordisk A/S
RecruitingPhase 32026-05-212500
A Research Study to Look at How Well CagriSema Helps People Living With Obesity Lose Weight and Maintain Weight Loss in the Long-term
NCT07011667 · Novo Nordisk A/S
Active, not recruitingPhase 32025-06-03609
A Research Study to See How Much CagriSema Lowers Blood Sugar and Body Weight Compared to Placebo in People With Type 2 Diabetes Treated With Diet and Exercise
NCT06323174 · Novo Nordisk A/S
CompletedPhase 32024-03-19189
A Research Study on How Well Cagrilintide and CagriSema Work in Children and Adolescents With Excess Body Weight
NCT07253285 · Novo Nordisk A/S
RecruitingPhase 32026-01-08460
A Research Study to See How Well CagriSema Helps People With Excess Body Weight Lose Weight
NCT05567796 · Novo Nordisk A/S
Active, not recruitingPhase 32022-11-013400
A Research Study to See if Kidney Damage in People With Chronic Kidney Disease and Type 2 Diabetes Living With Overweight or Obesity Can be Reduced by CagriSema Compared to Semaglutide, Cagrilintide and Placebo
NCT06131372 · Novo Nordisk A/S
CompletedPhase 22024-04-01626
A Research Study to Investigate the Effects of CagriSema Compared to Placebo in People With Type 2 Diabetes and Painful Diabetic Peripheral Neuropathy
NCT06797869 · Novo Nordisk A/S
CompletedPhase 22025-01-29142
A Study to See How Metabolism is Influenced by Weight Loss Due to Intervention With Cagrilintide and Semaglutide Compared to Diet
NCT07184086 · Novo Nordisk A/S
Active, not recruitingPhase 12025-09-2680
The Role of the Amylin Analogue Cagrilintide in Bone Metabolism
NCT07010432 · Novo Nordisk A/S
RecruitingPhase 12025-06-12144
A Research Study to See How Much CagriSema Lowers Blood Sugar and Body Weight Compared to Placebo in Children and Adolescents With Type 2 Diabetes
NCT07282613 · Novo Nordisk A/S
RecruitingPhase 32026-08-0480
A Research Study to See How Much CagriSema Lowers Blood Sugar and Body Weight Compared to Placebo in People With Type 2 Diabetes Treated With Once-daily Basal Insulin With or Without Metformin
NCT06323161 · Novo Nordisk A/S
CompletedPhase 32024-03-26274
A Research Study to See How Much CagriSema Lowers Blood Sugar and Body Weight Compared to Tirzepatide in People With Type 2 Diabetes Treated With Metformin, SGLT2 Inhibitor or Both
NCT06534411 · Novo Nordisk A/S
CompletedPhase 32024-11-051023
A Research Study to See How Much CagriSema Lowers Blood Sugar and Body Weight Compared to Tirzepatide in People With Type 2 Diabetes Treated With Metformin With or Without an SGLT2 Inhibitor
NCT06221969 · Novo Nordisk A/S
CompletedPhase 32024-01-161024

Desmopressin

StudyStatusPhaseStartPeople
FESS With or Without Intranasal Desmopressin in Chronic Rhinosinusitis With Nasal Polyps
NCT07855315 · Services Institute of Medical Sciences, Pakistan
Not yet recruitingNot applicable2026-10-15174
Prophylactic Desmopressin Before Native Kidney Biopsy in Severe Renal Impairment
NCT07840313 · Sindh Institute of Urology and Transplantation
CompletedNot applicable2017-08-01250
DDAVP Effect by TEG6 in Cardiac Surgery
NCT07179991 · London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
Recruiting2026-08-01100
Desmopressin Stimulation Test Performance in ACTH-Dependent Cushing Syndrome
NCT06635629 · National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
RecruitingPhase 22024-12-12140
Bedtime Device Restriction and Desmopressin in PMNE.
NCT07776977 · Al-Azhar University
RecruitingNot applicable2026-08-20140
Randomized Controlled Clinical Study on the Prophylactic Intraoperative Use of Desmopressin in Complex Sellar Region Tumors
NCT07712328 · Zhaoyun Zhang
Enrolling by invitationPhase 42026-06-02152
Bleeding Reduction in Acute and Chronic Kidney Patients Having Surgery (BRACKETS) Pilot Trial
NCT06337838 · Hamilton Health Sciences Corporation
RecruitingPhase 32025-06-09100
DDAVP for Pituitary Adenoma
NCT04569591 · National Institute of Neurological Disorders and Stroke (NINDS)
RecruitingNot applicable2026-03-0922
Vitamin D Versus Desmopressin Versus Combination Therapy in Children With Primary Monosymptomatic Nocturnal Enuresis and Vitamin D Deficiency
NCT07292753 · Ain Shams University
CompletedNot applicable2024-12-1590
Ginkgo Biloba vs Desmopressin in Treatment of Children With Monosymptomatic Nocturnal Enuresis
NCT06771128 · Menoufia University
CompletedNot applicable2024-11-01398
Omegapres Versus Solifenacin and Mirabegron Combination Therapy in Treatment of Primary MNE
NCT07199894 · Mansoura University
RecruitingPhase 32024-12-01120
Bleeding Prevention With Desmopressin for Allograft Kidney Biopsies
NCT06622187 · Hospital de Clinicas de Porto Alegre
Enrolling by invitationPhase 42024-08-1496
Uroflowmetry and Nocturnal Enuresis
NCT07028645 · Furkan Adem Canbaz
Active, not recruiting2022-08-20100
Transfusion Reduction in High-Bleeding-Risk Cardiac Surgery With Desmopressin
NCT07012837 · Imam Abdulrahman Bin Faisal University
Not yet recruitingPhase 32025-07112
Systematic Use of DDAVP to Prevent Serum Sodium Overcorrection in Severe Hyponatremia
NCT06020495 · Assistance Publique - Hôpitaux de Paris
RecruitingPhase 32024-12-17260

Teriparatide

StudyStatusPhaseStartPeople
Combined Anabolic Therapy
NCT06558188 · Massachusetts General Hospital
RecruitingPhase 42025-02-0350
PROactive HEALing in High-Risk Pelvic and Non-hip Lower Extremity Fragility Fractures (PRO HEAL Pilot)
NCT06303284 · University of Calgary
Not yet recruitingPhase 1 / Phase 22027-03-1554
Novel Combination Therapy for Osteoporosis in Men
NCT03994172 · VA Office of Research and Development
CompletedPhase 42019-07-0140
Bone Turnover Markers and Treatment Efficacy in Postmenopausal Osteoporosis
NCT07242612 · Khyber Medical University Peshawar
CompletedNot applicable2025-10-0140
Sequential Therapies After Osteoanabolic Treatment
NCT06164795 · 424 General Military Hospital
Recruiting2023-11-25150
Treatment of Osteogenesis Imperfecta With Parathyroid Hormone and Zoledronic Acid
NCT03735537 · University of Edinburgh
CompletedPhase 42016-11-01350
Teriparatide (Forsteo) Treatment in Postmenopausal Women: Mechanism of Action
NCT01293292 · Sheffield Teaching Hospitals NHS Foundation Trust
CompletedPhase 42011-0119
Novel Precision Medicine Approach to Treatment of Osteoporosis Based on Bone Turnover
NCT05151484 · Madhumathi Rao
Active, not recruitingPhase 42022-03-2160
Preoperative Teriparatide Use on Insertional Torque of Pedicle Screws for Lumbar Fusion Surgery
NCT03770338 · The University of Hong Kong
Active, not recruitingNot applicable2019-03-01192
Effects of Teriparatide (PTH) on Bone in Men and Women With Osteoporosis
NCT01155232 · University Health Network, Toronto
Active, not recruiting2004-11100
Teriparatide (PTH) and Bone Strength in Postmenopausal Women
NCT01155245 · University Health Network, Toronto
Active, not recruiting2008-0660
Precision Medicine Approach for Osteoporosis - Follow Up Study
NCT06264609 · Paul F Netzel
Enrolling by invitationPhase 42024-02-0140
Assess Safety and Compare PK of New Oral hPTH(1-34) Tablet Formulations vs. EBP05 Tablets and Subcutaneous Forteo
NCT05965167 · Entera Bio Ltd.
CompletedPhase 12023-05-1145
Study of the Key Techniques of Prevention and Treatment of Osteoporotic Refracture
NCT05866029 · Peking Union Medical College Hospital
RecruitingNot applicable2023-05-262478
Effect of Teriparatide, Vibration and the Combination on Bone Mass and Bone Architecture in Chronic Spinal Cord Injury
NCT01225055 · Thomas J. Schnitzer
CompletedPhase 22010-1060

Glucagon

StudyStatusPhaseStartPeople
Efficacy, Safety and Tolerability of Switching From Glucagon-like Peptide-1 Receptor Agonists (GLP-1RA) to Maridebart Cafraglutide in Adults With Obesity or Overweight (MARITIME-SWITCH)
NCT07575399 · Amgen
RecruitingPhase 32026-05-11300
Exploring the Influence of Glucagon-like Peptide -1 (GLP-1) Medications on Food Cravings, Food Selection, and Food Intake Following Exposure to Food Advertisements
NCT07505134 · Penn State University
Not yet recruitingNot applicable2026-0950
The Role of Glucagon in Glucose Metabolism in Humans With and Without Bariatric Surgery
NCT07212868 · The University of Texas Health Science Center at San Antonio
RecruitingPhase 12026-02-25150
Ellacor® Micro-Coring Technology® in Fitzpatrick Skin Types I-VI, Including Patients Receiving Glucagon-Like Peptide-1 Receptor Agonists
NCT07224880 · Cytrellis Biosystems, Inc.
Completed2025-10-149
Danish Trial of Weight Loss to Reduce Atrial Fibrillation Progression
NCT07816744 · Axel Brandes
Not yet recruitingNot applicable2026-10-01480
Glucagon-Like Peptide-1 Receptor Agonist in the Treatment of Adult, Obesity-related, Symptomatic Asthma (GATA-3)
NCT05254314 · Vanderbilt University Medical Center
Active, not recruitingPhase 22022-10-11100
Combination Therapy for Alcohol Use Disorder
NCT07249554 · Johns Hopkins University
Not yet recruitingPhase 22026-1145
A Pan-European Post-Authorisation Safety Study: Risk of Pancreatic Cancer Among Type 2 Diabetes Patients Who Initiated Exenatide as Compared With Those Who Initiated Other Non-Glucagon-Like Peptide 1 Receptor Agonists Based Glucose Lowering Drugs
NCT05663515 · AstraZeneca
Recruiting2024-09-3024000
Glucagon-like Peptide-1 Receptor Agonists for Endovascular Stroke Thrombectomy
NCT07511543 · Population Health Research Institute
Not yet recruitingPhase 22026-10-31100
Glucagon-like Peptide-1 Metabolism and Acute Neprilysin Inhibition
NCT03508739 · University of Pennsylvania
WithdrawnPhase 32018-06-010
Effects of Glucagon-like Peptide-1 (GLP-1) Agonist in Neuro-reproductive Function in Obese Adolescent Females With Polycystic Ovary Syndrome (PCOS)
NCT07169136 · Nemours Children's Clinic
Recruiting2025-09-1120
Post-Prandial Carbohydrate Metabolism in Individuals With and Without Post-Bariatric Surgery Hypoglycemia (PBH)
NCT07818707 · Joslin Diabetes Center
RecruitingPhase 42026-01-2740
A Study in People With Obesity to Test the Effects of BI 456906 Compared With Semaglutide on Glucagon Receptor Activity in the Liver
NCT05202353 · Boehringer Ingelheim
Active, not recruitingPhase 12024-11-0129
Graded Insulin Suppression Test P&F
NCT06592261 · Columbia University
RecruitingPhase 12024-09-1615
Glucagon-like Peptide-1 Receptor PET/CT in GLP-1R Related Disease
NCT06725693 · Tianjin Medical University
Recruiting2019-02-01500

Dulaglutide

StudyStatusPhaseStartPeople
A Study of Orforglipron (LY3502970) Compared With Dulaglutide in Pediatric Participants With Type 2 Diabetes
NCT07668336 · Eli Lilly and Company
Not yet recruitingPhase 32026-09170
Weekly GLP-1 Receptor Agonists in Obese Individuals Without Diabetes
NCT07834398 · Zagazig University
CompletedPhase 32025-11-14150
Comparative Study of Tirzepatide Versus Dulaglutide (SURPASS CVOT) or Semaglutide on Major Cardiovascular Events in Participants With Type 2 Diabetes
NCT06779929 · Brigham and Women's Hospital
Completed2024-11-0170000
Comparative Study of Different Weekly GLP-1 Receptor Agonists Among Diabetic and Non-Diabetic Patients: Clinical Trial
NCT07820111 · Zagazig University
CompletedPhase 32025-10-18159
Impact of Pharmacogenetic-Guided Treatment on Type 2 Diabetes.
NCT06851962 · Fundación para la Investigación del Hospital Clínico de Valencia
CompletedPhase 42025-05-2692
A Study to Evaluate the Effect of Fasting Duration and Dulaglutide (LY2189265) Withholding on Gastric Retention in Participants With Type 2 Diabetes Mellitus
NCT07313813 · Eli Lilly and Company
CompletedPhase 12025-12-2920
Therapeutic Strategies for Microvascular Dysfunction in Type 1 Diabetes
NCT05478707 · AdventHealth Translational Research Institute
RecruitingPhase 22023-10-0547
A Study of Dulaglutide (LY2189265) 3.0 mg and 4.5 mg in Pediatric Participants With Type 2 Diabetes Mellitus (AWARD-PEDS PLUS)
NCT06739122 · Eli Lilly and Company
RecruitingPhase 32025-01-1055
Emulation of the REWIND Cardiovascular Outcomes Trial in Healthcare Claims Data.
NCT07417631 · Brigham and Women's Hospital
Completed2026-02-03300000
INcreTin-based thERapies for Cardiovascular Event PrevenTion in Patients With and Without ASCVD (INTERCEPT-ASCVD)
NCT07417618 · Brigham and Women's Hospital
Completed2026-01-2760000
Injectable Semaglutide vs Dulaglutide in Individuals at Cardiovascular Risk
NCT07619495 · Brigham and Women's Hospital
Completed2026-01-20120000
A Study of Tirzepatide (LY3298176) Compared With Dulaglutide on Major Cardiovascular Events in Participants With Type 2 Diabetes
NCT04255433 · Eli Lilly and Company
CompletedPhase 32020-05-2913299
Phase II Study of Switching From Dulaglutide to PG-102(MG12) in Type 2 Diabetes Mellitus
NCT07677891 · ProGen. Co., Ltd.
Not yet recruitingPhase 22026-1060
Role of Glucagon-like Peptide-1 Receptor Agonists in Menstrual Irregularities in Adolescent Females With Type 1 Diabetes Mellitus
NCT07319286 · Ain Shams University
Enrolling by invitationPhase 1 / Phase 22025-08-0450
GLP-1 Agonist Therapy in Cystic Fibrosis-Related Glucose Intolerance
NCT04731272 · University of Pennsylvania
RecruitingPhase 22021-07-1630

Thymosin alpha-1

StudyStatusPhaseStartPeople
Thymalfasin for Immune Recovery in Adults With Sepsis
NCT07866118 · Shanghai Zhongshan Hospital
RecruitingNot applicable2026-10-0660
Study of Adebrelimab Combined With Thymalfasin and Chemotherapy for Neoadjuvant Treatment of Esophageal Cancer
NCT07780721 · The Affiliated Hospital of Putian University
Not yet recruitingPhase 22026-08-3031
Thymalfasin (Thymosin Alpha 1; Ta1) as an Enhancer of Vaccine Response Among Older Adults Receiving Booster Doses of COVID-19 Vaccine
NCT06821100 · The Methodist Hospital Research Institute
RecruitingPhase 12024-12-0275
Neoadjuvant Chemoradiotherapy Combined With PD-1 Inhibitor and Thymalfasin for Locally Advanced Mid-low Rectal Cancer
NCT06024356 · Beijing Friendship Hospital
Completed2023-09-2047
Thymosin Alpha 1 Combined With Anti-PD-1 Monoclonal Antibody in Elderly Patients With Advanced Melanoma
NCT07644897 · Sun Yat-sen University
RecruitingPhase 22023-05-3055
Thymosin Alpha 1 to Prevent COVID-19 Infection in Renal Dialysis Patients
NCT04428008 · William B. Ershler, MD
CompletedPhase 22021-01-12189
Phase II Trial of Neoadjuvant Thymalfasin, PD-1 Inhibitor, and Chemoradiotherapy for cStage III GEJ Adenocarcinoma
NCT07277439 · The First Affiliated Hospital with Nanjing Medical University
RecruitingPhase 22025-12-1648
Efficacy and Safety of Anti-PD-1, Thymalfasin, and SOX in Neoadjuvant Treatment of cStage III Gastric/Gastroesophageal Junction Adenocarcinoma
NCT06461910 · Zekuan Xu
RecruitingPhase 22024-06-1430
AI-assisted Subtyping-directed Precision Treatment in Acute Aortic Dissection
NCT07382375 · Nanjing Medical University
Not yet recruitingNot applicable2027-12-31300
Neoadjuvant Chemoradiotherapy Combined With PD-1 Inhibitor and Thymalfasin for pMMR/MSS Locally Advanced Mid-low Rectal Cancer
NCT06056804 · Beijing Friendship Hospital
Active, not recruitingPhase 22024-01-0320
"Thymalfasin Immunotherapy Study with Triple Regimen in Advanced MSS/pMMR Colorectal Cancer"
NCT06829355 · Beijing Friendship Hospital
RecruitingPhase 22025-02-1152
Neoadjuvant With Tα1 Plus Immuno-chemotherapy for Resectable NSCLC
NCT06607926 · Xuanwu Hospital, Beijing
Status unknownNot applicable2024-10-1540
Thymalfasin and Recombinant Human IL-2 Injections in Treating Lymphocytopenia for Patients With Malignant Hematological Tumors
NCT06584006 · The First Affiliated Hospital of Xiamen University
RecruitingPhase 22024-09-0150
Radiotherapy With Sequential Chemotherapy Combined With PD-1 Inhibitor and Thymalfasin for BRPC
NCT06573398 · Ruijin Hospital
Not yet recruitingPhase 22024-09-0120
Thymosin Alpha-1 for irAE Secondary to ICIs
NCT06178146 · Jun Wang
Status unknownPhase 42023-09-0140

Vosoritide

StudyStatusPhaseStartPeople
Study to Evaluate the Efficacy and Safety of BMN 333 Versus Vosoritide in Children With Achondroplasia
NCT07441876 · BioMarin Pharmaceutical
RecruitingPhase 2 / Phase 32026-04-20160
A Study of Vosoritide in Children With Noonan Syndrome With Inadequate Growth During or After Human Growth Hormone Treatment
NCT06668805 · BioMarin Pharmaceutical
Active, not recruitingPhase 22024-11-2230
Long-Term Extension Study of Vosoritide to Treat Children With Hypochondroplasia
NCT07073014 · BioMarin Pharmaceutical
Enrolling by invitationPhase 32025-06-20140
A Phase 2 Study of Vosoritide in Children With Idiopathic Short Stature
NCT06382155 · BioMarin Pharmaceutical
RecruitingPhase 22024-10-21100
A Study of Vosoritide Versus Placebo in Children With Hypochondroplasia Aged 0 to < 36 Months
NCT07126262 · BioMarin Pharmaceutical
RecruitingPhase 22025-07-3060
Vosoritide for Selected Genetic Causes of Short Stature
NCT04219007 · Andrew Dauber
Active, not recruitingPhase 22020-08-0456
A Study to Evaluate Long-Term Safety, Tolerability, & Efficacy of BMN 111 in Children With Achondroplasia (ACH)
NCT02724228 · BioMarin Pharmaceutical
Active, not recruitingPhase 22016-01-2630
A Clinical Trial to Evaluate Safety of Vosoritide in At-risk Infants With Achondroplasia
NCT04554940 · BioMarin Pharmaceutical
Active, not recruitingPhase 22020-10-1020
An Extension Study to Evaluate Safety and Efficacy of BMN 111 in Children With Achondroplasia
NCT03989947 · BioMarin Pharmaceutical
Active, not recruitingPhase 22019-06-1273
An Extension Study to Evaluate the Efficacy and Safety of BMN 111 in Children With Achondroplasia
NCT03424018 · BioMarin Pharmaceutical
Active, not recruitingPhase 32017-12-12119
Safety and Efficacy of Voxzogo for Growth Deficits in MPS IVA and VI
NCT05845749 · University of California, San Francisco
Active, not recruitingPhase 1 / Phase 22023-09-256
Interventional Study of Vosoritide for the Treatment of Children With Hypochondroplasia
NCT06455059 · BioMarin Pharmaceutical
Active, not recruitingPhase 32024-06-1780
Vosoritide for Short Stature in Turner Syndrome
NCT05849389 · Roopa Kanakatti Shankar, MBBS, MS
Status unknownPhase 22024-04-1220
A Clinical Trial to Evaluate the Safety and Efficacy of BMN 111 in Infants and Young Children With Achondroplasia
NCT03583697 · BioMarin Pharmaceutical
CompletedPhase 22018-06-1375
Bioequivalence Study to Compare Two Injection Devices for BMN 111 in Healthy Participants
NCT05813314 · BioMarin Pharmaceutical
TerminatedPhase 12023-03-1536

Survodutide

StudyStatusPhaseStartPeople
SYNCHRONIZE®-START- A Study to Test Whether Survodutide Helps People Living With Overweight or Obesity Who do Not Have Diabetes to Lose Weight
NCT07855900 · Boehringer Ingelheim
Not yet recruitingPhase 32026-11-07350
LIVERAGE™: A Study to Test Whether Survodutide Helps People With a Liver Disease Called NASH/MASH Who Have Moderate or Advanced Liver Fibrosis
NCT06632444 · Boehringer Ingelheim
RecruitingPhase 32024-10-141800
LIVERAGE™ - Cirrhosis: A Study to Test Whether Survodutide Helps People With a Liver Disease Called NASH/MASH Who Have Cirrhosis
NCT06632457 · Boehringer Ingelheim
RecruitingPhase 32024-11-121590
A Study to Test the Effect of Survodutide (BI 456906) on Cardiovascular Safety in People With Overweight or Obesity (SYNCHRONIZE™ - CVOT)
NCT06077864 · Boehringer Ingelheim
CompletedPhase 32023-11-205531
A Study to Test Whether Survodutide Helps People With Type 2 Diabetes Control Their Blood Sugar
NCT07754461 · Boehringer Ingelheim
RecruitingPhase 32026-08-24600
ELEVATE-LIVER: A Study to Test Whether Survodutide Helps Improve Heart Structure and Function in People With Overweight or Obesity and Fatty Liver Disease
NCT07850063 · Boehringer Ingelheim
Not yet recruitingPhase 32026-10-23600
SYNCHRONIZE®-HERA: A Study to Test Whether Survodutide Helps Women Who Are Living With Overweight or Obesity and Are Going Through or Have Finished Menopause, to Lose Weight
NCT07850050 · Boehringer Ingelheim
Not yet recruitingPhase 32026-10-31600
A Study in People With Overweight or Obesity to Compare How 2 Different Formulations of Survodutide Are Taken up by the Body
NCT07407348 · Boehringer Ingelheim
Active, not recruitingPhase 12026-03-1180
A Study to Compare How 2 Different Formulations of Survodutide Are Taken up in the Body When Given by Injection in Healthy Men and Women With and Without Overweight or Obesity
NCT07768813 · Boehringer Ingelheim
RecruitingPhase 12026-09-0244
A Study in People With Obesity to Test the Effects of BI 456906 Compared With Semaglutide on Glucagon Receptor Activity in the Liver
NCT05202353 · Boehringer Ingelheim
Active, not recruitingPhase 12024-11-0129
A Study to Test Whether Survodutide (BI 456906) Helps People Living With Overweight or Obesity Who Also Have Diabetes to Lose Weight
NCT06066528 · Boehringer Ingelheim
CompletedPhase 32023-11-27755
A Study in Healthy People to Compare How 2 Different Formulations of Survodutide Are Taken up by the Body
NCT07221591 · Boehringer Ingelheim
CompletedPhase 12025-11-05100
A Study in Healthy People or Otherwise Healthy With Overweight or Obesity to Compare 2 Formulations of Survodutide Given in Different Ways, Either as a Pre-filled Syringe or a Pen-like Injector
NCT07413913 · Boehringer Ingelheim
CompletedPhase 12026-03-0356
A Study to Test Whether Survodutide Improves How the Body Uses Energy and Breaks Down Fat in People With Obesity
NCT06745284 · Boehringer Ingelheim
Active, not recruitingPhase 12025-03-2664
A Study to Test Whether Survodutide Helps People Living With Obesity or Overweight and With a Confirmed or Presumed Liver Disease Called Non-alcoholic Steatohepatitis (NASH) to Reduce Liver Fat and to Lose Weight (SYNCHRONIZE-MASLD)
NCT06309992 · Boehringer Ingelheim
CompletedPhase 32024-04-02218

Retatrutide

StudyStatusPhaseStartPeople
A Master Protocol of Multiple Agents in Adults With Metabolic Dysfunction-Associated Steatotic Liver Disease (SYNERGY-Outcomes)
NCT07165028 · Eli Lilly and Company
RecruitingPhase 32025-10-154500
The Effect of Retatrutide Once Weekly on Cardiovascular Outcomes and Kidney Outcomes in Adults Living With Obesity (TRIUMPH-Outcomes)
NCT06383390 · Eli Lilly and Company
Active, not recruitingPhase 32024-04-3010000
A Study to Evaluate the Effect of Retatrutide on Insulin Secretion and Insulin Sensitivity in Adult Participants With Type 2 Diabetes Mellitus
NCT06982859 · Eli Lilly and Company
Active, not recruitingPhase 12025-06-0295
Effect of Retatrutide Compared With Semaglutide in Adult Participants With Type 2 Diabetes and Inadequate Glycemic Control With Metformin With or Without SGLT2 Inhibitor (TRANSCEND-T2D-2)
NCT06260722 · Eli Lilly and Company
Active, not recruitingPhase 32024-02-211250
A Study of Retatrutide (LY3437943) in Participants Who Have Obesity or Overweight and Chronic Low Back Pain
NCT07035093 · Eli Lilly and Company
Active, not recruitingPhase 32025-05-29586
A Study of Retatrutide (LY3437943) in Participants Who Have Obesity or Overweight
NCT05929066 · Eli Lilly and Company
CompletedPhase 32023-07-102335
Pre-approval Expanded Access of Retatrutide (LY3437943)
NCT07629401 · Eli Lilly and Company
AVAILABLE
A Study of Retatrutide (LY3437943) in Participants With Type 2 Diabetes Mellitus Who Have Obesity or Overweight
NCT05929079 · Eli Lilly and Company
CompletedPhase 32023-07-111152
A Study of Retatrutide (LY3437943) in Participants With Obesity and Cardiovascular Disease
NCT05882045 · Eli Lilly and Company
CompletedPhase 32023-05-301946
Effect of Retatrutide Compared With Placebo in Participants With Type 2 Diabetes and Moderate or Severe Renal Impairment, With Inadequate Glycemic Control on Basal Insulin, With or Without Metformin and/or SGLT2 Inhibitor (TRANSCEND-T2D-3)
NCT06297603 · Eli Lilly and Company
Active, not recruitingPhase 32024-03-15320
A Study of Retatrutide (LY3437943) Compared to Tirzepatide (LY3298176) in Adults Who Have Obesity
NCT06662383 · Eli Lilly and Company
Active, not recruitingPhase 32024-11-01800
A Study to Investigate the Response of Participants With Type 2 Diabetes Mellitus on Once-Weekly Retatrutide to Hypoglycemia
NCT06982846 · Eli Lilly and Company
CompletedPhase 12025-06-0680
A Study of Retatrutide (LY3437943) in Participants Without Type 2 Diabetes Who Have Obesity or Overweight
NCT07357415 · Eli Lilly and Company
Active, not recruitingPhase 32026-01-24600
A Study of Retatrutide (LY3437943) in Participants With Obesity or Overweight
NCT07232719 · Eli Lilly and Company
Active, not recruitingPhase 32025-11-17250
Effect of LY3437943 Versus Placebo in Participants Who Have Obesity or Are Overweight
NCT07467447 · Hudson Biotech
RecruitingPhase 22026-02-15300

Cerebrolysin

StudyStatusPhaseStartPeople
Combined Acupuncture-Based Therapy for Rehabilitation After Ischemic Stroke
NCT07846488 · National Hospital of Acupuncture, Vietnam
Not yet recruitingNot applicable2026-12-01440
Cerebrolysin After Reperfusion in Extended-window EndoVascular Thrombectomy
NCT06339411 · Chang Gung Memorial Hospital
Not yet recruitingPhase 22026-09-01100
Efficacy and Safety of Cerebrolysin on Prolonged Disorders of Consciousness
NCT04427241 · Konkuk University Medical Center
RecruitingPhase 42023-06-0112
Combined Cerebrolysin and Amantadine Sulfate Administration for Patients With Traumatic Brain Injury in the ICU
NCT06052787 · Ain Shams University
CompletedPhase 32023-09-01150
Efficacy of Prednisolone Versus Cerebrolysin in the Treatment of Bell's Palsy
NCT05821075 · October 6 University
RecruitingPhase 1 / Phase 22023-08-2490
Cerebrolysin in Early Stroke Rehabilitation - Tertiary Study
NCT07043686 · University Medical Centre Ljubljana
RecruitingNot applicable2025-06-1330
Safety and Feasibility of Using Cerebrolysin in the Treatment of Primary Intracerebral Hemorrhage - a Prospective Randomized Open Blinded End-point Trial
NCT06899464 · Cardinal Stefan Wyszynski University
Not yet recruitingPhase 42025-10-0130
Effects of Cerebrolysin on Language Ability in Non-fluent Aphasia Patients After Stroke: A Randomized, Placebo-controlled, Double-blinded, Single Center Study
NCT06897176 · Yonsei University
RecruitingPhase 42025-03-1240
Cerebrolysin REGistry Study in Stroke - a High-quality Observational Study of Comparative Effectiveness
NCT03480698 · Ever Neuro Pharma GmbH
Completed2018-04-241851
CERebrolysin In CADASIL
NCT05755997 · Ever Neuro Pharma GmbH
Active, not recruitingPhase 22023-11-2930
Cerebrolysin in Critically Ill Patients With Delirium
NCT06677502 · Medical University of Lublin
Enrolling by invitationNot applicable2024-01-01500
Clinical Characteristics and Treatment of Anosmia and Ageusia Due to SARS-CoV2 Variants
NCT06208540 · Sherifa Ahmed Hamed
CompletedPhase 42021-08-30160
Cerebrolysin as an Add-On Therapy to Standard Treatment of Basilar Artery Occlusion
NCT06489925 · University Hospital Sestre Milosrdnice
Status unknownEarly phase 12024-0720
Cerebrolysin in SAH (Subarachnoidal Haemorrhage) - Observational Study
NCT06429943 · Pomeranian Medical University Szczecin
Completed2021-01-1547
Effect of Cerebrolysin on the Blood Brain Barrier in Patients With Diabetes and Ischemic Stroke
NCT06273020 · Hospital Universitario Dr. Jose E. Gonzalez
Status unknownPhase 42022-11-1760

Bivalirudin

StudyStatusPhaseStartPeople
Multicenter Trial of ECMO in Children With Severe Cardiac Failure Using the Cardiohelp System
NCT06080074 · Stanford University
RecruitingPhase 22025-04-1550
BivaLirudin versUS Heparin in Extracorporeal Membrane Oxygenation
NCT05959252 · Sydney Local Health District
RecruitingPhase 22024-05-0180
Use of Bivalirudin for Anticoagulation in Patients With Extracorporeal Membrane Oxygenation
NCT06275555 · Xiaotong Hou
RecruitingNot applicable2024-06-03154
Bivalirudin Versus Heparin During PCI in High Bleeding Risk Patients With Acute Coronary Syndromes
NCT07383155 · Shenyang Northern Hospital
Not yet recruitingPhase 42026-02-015270
A Single Center Diagnostic, Cross-sectional Study of Coronary Microvascular Dysfunction
NCT03537586 · NYU Langone Health
Active, not recruitingNot applicable2018-06-29206
Bivalirudin With Prolonged Full Dose Infusion Versus Heparin Alone During Emergency PCI
NCT03822975 · Shenyang Northern Hospital
CompletedNot applicable2019-02-146016
A Study on the Impact of Bivalirudin Usage During PCI for High-risk Plaques on Post-PCI Coronary Microcirculation.
NCT05984537 · Peking University First Hospital
RecruitingPhase 42023-07-0170
Pharmacokinetics of Bivalirudin for Pediatric Anticoagulation
NCT03532399 · Boston Children's Hospital
Recruiting2018-07-1230
Bivalirudin with Prolonged Infusion During PCI Versus Heparin After Fibrinolytic Therapy
NCT06861374 · First Affiliated Hospital Xi'an Jiaotong University
Not yet recruitingNot applicable2025-052400
Comparison of Anticoagulation Prolongation vs. no Anticoagulation in STEMI Patients After Primary PCI
NCT03664180 · Beijing Anzhen Hospital
CompletedPhase 42019-01-112989
Study Comparing Bivalirudin Versus Heparin in Neonatal and Pediatric ECMO
NCT03318393 · University of Texas Southwestern Medical Center
CompletedPhase 42018-03-2530
Bivalirudin Versus Enoxaparin in Critically Ill COVID-19 Patients
NCT05334654 · University Magna Graecia
CompletedNot applicable2022-04-2058
Safety and Efficacy of Prolonged Use of Bivalirudin 4 Hours After ePCI (COBER Study)
NCT04120961 · Nanjing First Hospital, Nanjing Medical University
CompletedNot applicable2019-09-20330
Safety and Efficacy of Bivalirudin During Short-term Intervention of Non-infarction Related Artery After PPCI of STEMI
NCT04475835 · First Affiliated Hospital Xi'an Jiaotong University
Status unknownNot applicable2021-01-12100
Reduce Bolus Injection of Bivalirudin
NCT03588611 · Han Yaling, MD
CompletedPhase 42019-10-01204

Enlicitide

StudyStatusPhaseStartPeople
A Study of Enlicitide Decanoate (MK-0616, an Oral PCSK9 Inhibitor) in Children and Adolescents With Heterozygous Familial Hypercholesterolemia (MK-0616-029)
NCT07058077 · Merck Sharp & Dohme LLC
RecruitingPhase 2 / Phase 32025-08-21153
A Clinical Trial of MK-7262 and Enlicitide in Participants With High Lipoprotein(a) (MK-7262-004)
NCT07614984 · Merck Sharp & Dohme LLC
RecruitingPhase 22026-06-30750
Enlicitide Decanoate (MK-0616 Oral PCSK9 Inhibitor) Renal Impairment Study (MK-0616-020)
NCT05934292 · Merck Sharp & Dohme LLC
CompletedPhase 12023-07-2033
A Clinical Study of MK-7262 and Enlicitide in Healthy Participants (MK-7262-003)
NCT07619443 · Merck Sharp & Dohme LLC
CompletedPhase 12026-07-0130
A Study of Enlicitide Decanoate (MK-0616 Oral PCSK9 Inhibitor) in Adults With Hypercholesterolemia (MK-0616-013) CORALreef Lipids
NCT05952856 · Merck Sharp & Dohme LLC
CompletedPhase 32023-08-102912
A Clinical Trial of Enlicitide and Rosuvastatin in Healthy Adults (MK-0616-039)
NCT07300280 · Merck Sharp & Dohme LLC
Active, not recruitingPhase 12025-12-2960
A Clinical Trial of Enlicitide (MK-0616) Formulations in Healthy Participants (MK-0616-044)
NCT07776665 · Merck Sharp & Dohme LLC
Active, not recruitingPhase 12026-08-3130
A Clinical Study of Enlicitide (MK-0616) in Adults With Hyperlipidemia in India (MK-0616-038)
NCT07821944 · Merck Sharp & Dohme LLC
Not yet recruitingPhase 32026-10-16150
A Clinical Study of Enlicitide in Participants With High Cholesterol (MK-0616-037)
NCT07216482 · Merck Sharp & Dohme LLC
Active, not recruitingPhase 32025-11-11996
A Study of Enlicitide Chloride (MK-0616 Oral PCSK9 Inhibitor) in Participants With Moderate Renal Impairment (MK-0616-007)
NCT05070390 · Merck Sharp & Dohme LLC
CompletedPhase 12021-11-1618
A Clinical Study of the Effect of Enlicitide (MK-0616) Formulations in Healthy Participants (MK-0616-041)
NCT07481708 · Merck Sharp & Dohme LLC
CompletedPhase 12026-03-2330
A Clinical Study of Enlicitide Decanoate in People With Liver Function Problems (MK-0616-030)
NCT06575959 · Merck Sharp & Dohme LLC
CompletedPhase 12024-09-2020
Enlicitide Decanoate (MK-0616 Oral PCSK9 Inhibitor) Cardiovascular Outcomes Study (MK-0616-015) CORALreef Outcomes
NCT06008756 · Merck Sharp & Dohme LLC
Active, not recruitingPhase 32023-10-0914550
A Study to Evaluate the Efficacy and Safety of Enlicitide (MK-0616, Oral PCSK9 Inhibitor) Compared With Ezetimibe or Bempedoic Acid or Ezetimibe and Bempedoic Acid in Adults With Hypercholesterolemia (MK-0616-018/CORALreef AddOn)
NCT06450366 · Merck Sharp & Dohme LLC
CompletedPhase 32024-07-08301
A Study of Enlicitide Decanoate (MK-0616 Oral PCSK9 Inhibitor) in Adults With Heterozygous Familial Hypercholesterolemia (MK-0616-017/CORALreef HeFH)
NCT05952869 · Merck Sharp & Dohme LLC
CompletedPhase 32023-08-08303

Calcitonin salmon

StudyStatusPhaseStartPeople
Beijing Osteoporosis With Neurological Disorders in Epigenetic Changes Study
NCT03401619 · Peking University Third Hospital
Active, not recruiting2017-09-212000
Subcutaneous Calcitonin in Acute Herpes Zoster
NCT07655804 · Tanta University
RecruitingPhase 32026-07-01168
Calcitonin Gene-related Peptide Antibody in Acute Mountain Sickness
NCT07653516 · Insel Gruppe AG, University Hospital Bern
Not yet recruitingPhase 42027-06-0130
Paravertebral Calcitonin in Thoracotomy
NCT06330168 · Tanta University
CompletedNot applicable2024-03-2892
Calcitonin Therapy on Incidence and Severity of Neuropathic Pain After Spinal Cord Injury
NCT05805683 · Tanta University
RecruitingNot applicable2023-05-01126
Plasma Calcitonin Gene-Related Peptide (CGRP) Levels in Patients With Head and Neck Malignancies Undergoing Radiotherapy
NCT07029373 · West China Hospital
Completed2025-07-0423
Induction of Migraine Attacks With Aura Using Calcitonin Gene-Related Peptide
NCT07021859 · Danish Headache Center
RecruitingNot applicable2025-06-2721
Adding Calcitonin to Bupivacaine in Transversalis Fascia Plane Block for Cesarean Section
NCT07033104 · Tanta University
RecruitingNot applicable2025-04-0170
Efficacy of Coadministration of Calcitonin and Hyperbaric Bupivacaine in Spinal Anesthesia in Tramadol-abuse Patients
NCT04445857 · Ain Shams University
CompletedPhase 42020-09-0190
Ultrasound Guided Block of Stellate Ganglion Versus Greater Occipital Nerve in Resistant Migraine and Correlation to Calcitonin Gene Related Peptide
NCT06662461 · Ain Shams University
RecruitingNot applicable2024-02-0140
Calcitonin Pre-treatment to Improve SPECT-CT Sensitivity
NCT03935984 · Joseph Sferra
RecruitingPhase 42019-05-2937
Evaluation of the Levels of Calcitonin Gene-related Peptide and Substance P
NCT06510751 · Melike Cengiz
Status unknown2024-03-0151
The Use of Intranasal Calcitonin to Improve Pain and Activity in Elderly Pelvic Ring Injuries
NCT03812991 · University of Missouri-Columbia
CompletedPhase 42019-07-0121
Evaluate the Safety and Efficacy of Calcitonin Gene-Related Peptide (CGRP) Antagonists in Patients With Dry Eye Disease and Asthenopia
NCT05895500 · Nvision Laser Eye Centers
Completed2023-05-10103
The Lacosamide's Effect on Calcitonin Gene-related Peptide in Migraine Patients
NCT05632133 · Kafrelsheikh University
CompletedPhase 32022-06-01200

HCG

StudyStatusPhaseStartPeople
Dual Trigger VS HCG Trigger for Final Oocyte Maturation in Normal Responders
NCT07861399 · Al-Azhar University
RecruitingNot applicable2026-09-01100
Evaluation of the Role of Luteinizing Hormone (LH) and Human Chorionic Gonadotropin (hCG) in Adult Patients Undergoing Assessment for Endocrine Disorders
NCT07824102 · Martin Blomberg Jensen
Recruiting2026-01-0120000
Ovulation Trigger Strategies in Low Ovarian Reserve (TRIGGERBEST)
NCT07816562 · Fundación para la Investigación del Hospital Clínico de Valencia
RecruitingPhase 32024-09-17126
Purpose to Evaluate the Effectiveness of the Superovulation Stimulation Protocol Using Human Chorionic Gonadotropin (hCG) by Demonstrating Its Equivalence to Standard Controlled Ovarian Stimulation Protocols in Terms of Oocytes Retrieved, Blastulation While Maintaining an Economic Advantage
NCT07771283 · LTD "EKODNIPRO", Medical centre Medical Plaza Dnipro
Enrolling by invitationNot applicable2026-08-17360
The Application of HCG in Luteal Support for Frozen Embryo Transfer in Ovulation Cycle of Obese Women
NCT07633002 · The Second Hospital of Shandong University
Not yet recruitingNot applicable2026-07-01750
Sex Steroids Balance for Metabolic and Reproductive Health in Klinefelter Syndrome
NCT05586802 · Georgios Papadakis
RecruitingPhase 32023-03-21150
Ruxolitinib, Human Chorionic Gonadotropin (uhCG/EGF), and Dose De-escalated Corticosteroids
NCT05123040 · Masonic Cancer Center, University of Minnesota
TerminatedPhase 1 / Phase 22023-06-0510
Retrospective Study of High Dose Follitropin Delta in a Mixed Protocol With Human Chorionic Gonadotropin
NCT05873725 · Clinique Ovo
Completed2023-05-20118
Effects of Intrauterine Flushing With Human Chorionic Gonadotropin on ICSI Outcome
NCT06684951 · Omayma Ismail Khalaf
CompletedPhase 42022-10-2390
Oxytocin Versus Human Chorionic Gonadotropin as Trigger in Ovulation Induction
NCT06725004 · Shakeela Ishrat
CompletedPhase 32023-01-0160
Efficacy of Human Chorionic Gonadotropin in Acute GVHD Treatment
NCT06904599 · Hospital Universitario Dr. Jose E. Gonzalez
RecruitingPhase 22025-02-0120
The Study of Human Chorionic Gonadotropin (HCG) Activating the Dormant Follicles .
NCT06754332 · The Fourth Affiliated Hospital of Zhejiang University School of Medicine
Not yet recruitingPhase 12025-04-0160
Calciotropic Effects After HCG Stimulation Test
NCT03254641 · Martin Blomberg Jensen
Completed2017-04-01242
Frozen-thawed Embryo Transfer in a Natural Cycle: hCG Triggering Versus LH Home Test
NCT03115320 · Tampere University Hospital
TerminatedPhase 42017-0162
HUMAN CHORIONIC GONADOTROPIN (HcG) VS MAGNESIUM SULPHATE (MgSo4) AS A TOCOLYTIC AGENT- A RANDOMIZED CONTROLLED TRIAL
NCT05828966 · Shaheed Zulfiqar Ali Bhutto Medical University
CompletedNot applicable2023-02-1570

Terlipressin

StudyStatusPhaseStartPeople
Terlipressin vs. Somatostatin in Cirrhotic Patients With Acute Variceal Bleeding and Renal Dysfunction
NCT07252401 · General Hospital of Shenyang Military Region
Not yet recruitingNot applicable2026-09-2564
Terlipressin vs Placebo to Reduce Bleeding in Fibroid Surgery
NCT07746349 · Sevil Cankaya
Not yet recruitingNot applicable2026-08-0180
Intraoperative Continuous Terlipressin Infusion is Associated With Reduced Severe Postoperative Complications After Laparoscopic Hepatectomy: a Prospective Propensity Score-matched Cohort Study
NCT07719933 · First Affiliated Hospital, Sun Yat-Sen University
Completed2024-04-01161
Effect of Terlipressin for Intraoperative Blood Pressure Management in Kidney Transplantation
NCT06855758 · Beijing Friendship Hospital
Active, not recruitingNot applicable2025-03-06150
Interest of in Situ Terlipressin Administration Before the Realisation of Bronchial Biopsy
NCT02970175 · University Hospital, Rouen
CompletedPhase 32017-06-30130
Effects of Terlipressin and Somatostatin on Portal Pressure in Patients Undergoing Living Donor Liver Transplantation
NCT07304466 · Istanbul Medipol University Hospital
RecruitingNot applicable2025-12-2950
ACid Tranexamic or Terlipressin for Initial Emergency Treatment of Mild to seVere hEmoptysis: a Randomized Trial.
NCT04961528 · Assistance Publique - Hôpitaux de Paris
CompletedPhase 32022-03-27315
Endothelin Receptor Antagonism With Ambrisentan to Treat Hepatorenal Syndrome
NCT06256432 · Noorik Biopharmaceuticals AG
Active, not recruitingPhase 22024-04-1754
Comparison of Terlipressin Versus Octreotide in Patients With Hepatorenal Syndrome
NCT07460908 · Lahore General Hospital
CompletedNot applicable2025-05-0160
Terlipressin in Combined Hepatorenal Syndrome in Patients With Signs of Chronic Renal Disease
NCT06161766 · University Hospital Freiburg
Completed2024-03-03490
Efficacy and Safety of Continuous Infusion of Terlipressin vs Bolus Terlipressin in ACLF Patients With Acute Esophageal Variceal Bleed
NCT06815770 · Institute of Liver and Biliary Sciences, India
Not yet recruitingPhase 2 / Phase 32025-02-1060
Terlipressin for HRS-AKI in Liver Transplant Candidates (INFUSE)
NCT04460560 · University of Pennsylvania
CompletedPhase 32020-12-1150
Safety and Efficacy of Continuous Infusion of Terlipressin With Norepinephrine Versus Norepinephrine Alone in Improving Outcomes of Acute Kidney Injury in Acute on Chronic Liver Failure With Septic Shock
NCT06556472 · Institute of Liver and Biliary Sciences, India
Status unknownNot applicable2024-08-15126
The Effect of Intramyometrial Injection of Terlipressin Versus Carbitocin on Hemoglobin and Blood Loss During Open Myomectomy Operations Using Haemostatic Tourniquets:
NCT05242783 · Wael Elbanna Clinic
CompletedNot applicable2022-02-0199
The Effect of Intracapsular Injection of Terlipressin Versus Carbitocin on Hemoglobin and Blood Loss During Laparoscopic Myomectomy Operations
NCT05170230 · Wael Elbanna Clinic
Status unknownNot applicable2022-02-2799

Linaclotide

StudyStatusPhaseStartPeople
Linaclotide in Treating Patients With Stages 0-3 Colorectal Cancer
NCT03796884 · Sidney Kimmel Comprehensive Cancer Center at Thomas Jefferson University
Active, not recruitingPhase 22019-10-30150
MRI Parameters as Biomarkers in Cystic Fibrosis (FEMPTO)
NCT07780344 · University of Nottingham
Not yet recruitingNot applicable2026-0912
A Study of Virtual Reality and Linaclotide for IBS-C
NCT05796388 · Mayo Clinic
RecruitingNot applicable2024-05-3165
A Study to Assess Adverse Events and Change in Symptoms With Linaclotide Versus Placebo in Pediatric Subjects, Ages 2 to 5 Years, With Functional Constipation
NCT05652205 · AbbVie
CompletedPhase 32022-12-29123
Proof of Principle Study for an Efficacy Trial of Linaclotide for Cystic Fibrosis
NCT07569419 · University of Nottingham
RecruitingEarly phase 12026-03-0926
GCC Agonist Signal in the Small Intestine
NCT05107219 · University of Wisconsin, Madison
CompletedPhase 12022-11-3043
Efficacy of Linaclotide in Type II Diabetics With Chronic Constipation
NCT03119584 · Texas Tech University Health Sciences Center, El Paso
Active, not recruitingPhase 42015-09-0123
"Efficacy and Safety of Linaclotide in Chronic Constipation"
NCT07431957 · Md Mehedi Shahriar
Not yet recruitingPhase 42026-02-2090
Linaclotide for Colonoscopy Bowel Prep
NCT06692673 · University of Florida
RecruitingPhase 1 / Phase 22025-12-0110
A Study to Assess Adverse Events and Change in Disease Activity in Pediatric Participants (Age 6 Months to <2 Years) With Functional Constipation Who Are Treated With Linaclotide
NCT05760313 · AbbVie
CompletedPhase 22023-04-2719
Long-term Safety of Linaclotide in Pediatric Participants With FC or IBS-C
NCT04166058 · AbbVie
CompletedPhase 32019-11-19381
Effect to Linaclotide on Colonic Motility
NCT06989268 · Universitaire Ziekenhuizen KU Leuven
CompletedPhase 42014-02-1010
Clinical Study on the Application of Lactulose Combined with Linaclotide in Bowel Preparation for Colonoscopy
NCT06748638 · Haifeng Lan
Status unknownPhase 42024-09-01444
Clinical Study of Bowel Preparation Before Colonoscopy
NCT06091735 · Jinling Hospital, China
CompletedNot applicable2023-08-01444
Linaclotide Acetate in Preventing Colorectal Cancer in Healthy Volunteers
NCT01950403 · Mayo Clinic
CompletedPhase 12013-0924

Abaloparatide

StudyStatusPhaseStartPeople
Abaloparatide vs. Placebo in Post-Menopausal Women and Abaloparatide in Men Receiving Initial Spinal Fusion Surgery
NCT03841058 · Hospital for Special Surgery, New York
Active, not recruitingPhase 22019-08-1496
The Effect of Osteoporotic Medications on Vertebral Bone Quality Score
NCT07587775 · State University of New York at Buffalo
Enrolling by invitationPhase 22026-06-1860
Sequential Therapies After Osteoanabolic Treatment
NCT06164795 · 424 General Military Hospital
Recruiting2023-11-25150
Abaloparatide Added to Ongoing Denosumab vs Continued Denosumab Alone
NCT04467983 · Hospital for Special Surgery, New York
Active, not recruitingPhase 42021-02-0170
Abaloparatide Before Total Knee Arthroplasty
NCT04167163 · University of Wisconsin, Madison
CompletedPhase 42020-01-1058
MicroRNA and Markers and Therapeutic Response to Romosozumab and Abaloparatide in Postmenopausal Osteoporosis
NCT07616401 · Istituto Auxologico Italiano
RecruitingNot applicable2025-08-3142
To Evaluate the Efficacy and Safety of Abaloparatide Injection (QLG2128) in the Treatment of Postmenopausal Women With Osteoporosis and at High Risk of Fracture
NCT06898060 · Qilu Pharmaceutical Co., Ltd.
Not yet recruitingPhase 32025-06282
A Single-center, Open, Randomized, Single-dose, Cross-over Bioequivalence Study to Evaluate the Effects of the Test Formulation Abalparatide Injection and the Reference Formulation Abalparatide Injection (Tymlos®) in Healthy Adult Subjects
NCT06753864 · The Affiliated Hospital of Qingdao University
Not yet recruitingPhase 12025-01-0232
PTH Analog Type II Odontoid Fracture
NCT04760782 · David Lunardini
TerminatedPhase 22022-05-1822
Abaloparatide and Pelvic Fracture Healing
NCT04249232 · Hospital for Special Surgery, New York
CompletedPhase 22020-09-1748
Supracondylar Distal Femur Fractures and Abaloparatide
NCT04626141 · Daniel Horwitz
WithdrawnPhase 42024-060
Real-world Effectiveness and Cardiovascular Safety Study of Abaloparatide in Postmenopausal Women
NCT04974723 · Radius Health, Inc.
Completed2021-07-0122054
Study to Evaluate the Pharmacokinetics (PK), Pharmacodynamics (PD), and Usability of Abaloparatide-solid Microstructured Transdermal System (sMTS) in Postmenopausal Women With Low Bone Mineral Density (BMD)
NCT04366726 · Radius Health, Inc.
CompletedPhase 12019-04-0922
Safety and Efficacy of Abaloparatide-SC in Men With Osteoporosis (ATOM)
NCT03512262 · Radius Health, Inc.
CompletedPhase 32018-05-03228
Efficacy & Safety of Abaloparatide-Solid Microstructured Transdermal System in Postmenopausal Women With Osteoporosis
NCT04064411 · Radius Health, Inc.
CompletedPhase 32019-08-05511

Cosyntropin

StudyStatusPhaseStartPeople
Subclinical Primary Aldosteronism in Diabetes At-Risk for Kidney Disease
NCT06190158 · Brigham and Women's Hospital
Active, not recruitingEarly phase 12024-05-15125
Screening and Stimulation Testing for Residual Secretion of Adrenal Steroid Hormones in Autoimmune Addison's Disease
NCT03793114 · University of Bergen
Active, not recruitingNot applicable2018-09-26200
Updated Diagnostic Cortisol Values for Adrenal Insufficiency
NCT05149638 · Montefiore Medical Center
RecruitingNot applicable2022-02-0390
Positron Emission Tomography (PET) Imaging of Cholesterol Trafficking: Clinical Evaluation of [18F]FNP-59 in Normal Human Subjects (Groups 2, 3 & 4)
NCT04546126 · Benjamin Viglianti
RecruitingEarly phase 12021-11-0124
Stress and the Nervous System
NCT02339506 · Brigham and Women's Hospital
CompletedNot applicable2015-0423
Hormonal Mechanisms of Sleep Restriction - Axis Study
NCT03142893 · Peter y. Liu
Active, not recruitingPhase 12017-05-0880
Hormonal Mechanisms of Sleep Restriction - Axis Study in Older Men and Postmenopausal Women
NCT04037605 · Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center
Active, not recruitingEarly phase 12020-02-095
Evaluation of the Effectiveness and Tolerance of Tetracosactide Synacthen® in the Treatment of Post Dural Puncture Headaches (ESYBRECHE)
NCT02813655 · Hospices Civils de Lyon
TerminatedPhase 22016-1046
Defining the Mechanisms Underlying Adrenal Insufficiency in Cirrhosis
NCT04642391 · University of Virginia
Completed2021-08-0276
NeSST2: The Development of a Noninvasive Short Synacthen Test
NCT03514589 · Sheffield Children's NHS Foundation Trust
RecruitingPhase 22012-10-1212
Adrenocorticotropic Hormone Stimulation in Postural Orthostatic Tachycardia Syndrome (POTS)
NCT01764711 · Vanderbilt University
CompletedNot applicable2013-0113
Is Adrenal Insufficiency Under-diagnosed in Hospitalized Cirrhosis Patients?
NCT03368066 · University of Virginia
CompletedPhase 32018-01-29100
A Novel Approach to Infantile Spasms
NCT03347526 · University of Colorado, Denver
SuspendedPhase 32018-04-19394
Comparison of Intramuscular and Intravenous ACTH Stimulation Test in Normal Volunteers
NCT03752190 · Johns Hopkins University
WithdrawnPhase 42019-070
Effect of Adrenocorticotropic Hormone on Vascular Endothelial Growth Factor Release in Children Study
NCT03709381 · Nationwide Children's Hospital
CompletedEarly phase 12017-10-0110

Lanreotide

StudyStatusPhaseStartPeople
Study of RYZ101 Compared With SOC in Pts w Inoperable SSTR+ Well-differentiated GEP-NET That Has Progressed Following 177Lu-SSA Therapy
NCT05477576 · RayzeBio, Inc.
Active, not recruitingPhase 32022-03-24343
Randomized Interval Assessment Trial of Lu177-Dotatate in Slowly Progressive G1-2 Advanced Midgut Neuroendocrine Tumors
NCT06878664 · Grupo Espanol de Tumores Neuroendocrinos
RecruitingPhase 32025-06-12166
A Trial to Assess Efficacy and Safety of Octreotide Subcutaneous Depot in Patients With GEP-NET
NCT05050942 · Camurus AB
Active, not recruitingPhase 32021-10-22332
Cabozantinib and Lanreotide as Treatment for Gastroenteropancreatic Neuroendocrine Tumors
NCT05048901 · National Health Research Institutes, Taiwan
RecruitingPhase 1 / Phase 22021-09-1749
Lanreotide In Polycystic Kidney Disease Study
NCT02127437 · Assistance Publique - Hôpitaux de Paris
CompletedPhase 32014-09-19159
Lanreotide Versus Placebo Before Surgery to Prevent a Surgical Complication Called a Pancreatic Fistula
NCT06807437 · SWOG Cancer Research Network
RecruitingPhase 32025-05-09274
LAnreotide in Metastatic Pheochromocytoma / PARAganglioma (LAMPARA)
NCT03946527 · Antonio Fojo
Active, not recruitingPhase 22019-06-1710
A Study to Assess the Pharmacokinetics, Pharmacodynamics, Safety, and Tolerability of Debio 4126 in Participants With Acromegaly or Functioning Gastroenteropancreatic Neuroendocrine Tumors (GEP-NETs)
NCT05364944 · Debiopharm International SA
TerminatedPhase 12022-05-1819
A Study to Evaluate Patient Experience in the Therapy of Neuroendocrine Tumors Treated With Octreotide Long Acting Release Versus Lanreotide
NCT03289741 · Memorial Sloan Kettering Cancer Center
CompletedPhase 42017-09-1951
Study of Lanreotide Autogel in Non-functioning Entero-pancreatic Endocrine Tumours
NCT00353496 · Ipsen
CompletedPhase 32006-06264
Real-World Study (RWS) of Lanreotide Autogel (LAN) for the Treatment of Patients With Acromegaly in China
NCT05431803 · Ipsen
Completed2022-06-30129
Asian Investigation of Lanreotide Autogel® in the Management of GEP-NETs
NCT04696042 · Asan Medical Center
Completed2021-01-0171
United Kingdom (UK) Patient Preference Study of Somatuline Autogel and Treatment Administration Setting
NCT04649580 · Ipsen
Completed2021-04-2780
Study to Assess the Efficacy and Safety of Lanreotide Autogel® in Chinese Participants With GEP-NETs
NCT04852679 · Ipsen
CompletedPhase 32021-05-2443
Acromegaly Resistant to Conventional Dose of First Generation Somatostatin Ligands
NCT06607666 · Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Completed2023-01-26102

Pasireotide

StudyStatusPhaseStartPeople
Managing Pasireotide-associated Hyperglycaemia in Acromegaly With Ketogenic Diet
NCT07866846 · Leiden University Medical Center
RecruitingNot applicable2025-07-2930
Pasireotide s.c. in Patients With Post-Bariatric Hypoglycaemia
NCT05928390 · RECORDATI GROUP
Active, not recruitingPhase 22024-01-0493
A Study of Pasireotide in People With Prolactinoma
NCT06295952 · Memorial Sloan Kettering Cancer Center
RecruitingPhase 22024-02-2710
Study in Healthy Subjects to Investigate the Relative Bioavailability and Safety of Pasireotide After Single Subcutaneous Dose Administration Using a Reusable ServoPen With Cartridge as Compared to Administration Using a Syringe Drawn From an Ampule
NCT07312643 · RECORDATI GROUP
CompletedPhase 12025-12-0140
Reduction by Pasireotide of the Effluent Volume in High-output Enterostomy in Patients Refractory to Usual Medical Treatment
NCT02713776 · Hospices Civils de Lyon
CompletedPhase 22016-12-1357
Effects of Pasireotide Lar Therapy on Bone Metabolism
NCT07179926 · Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Recruiting2025-09-08120
Pasireotide (SOM230) With or Without Everolimus in Treating Patients With Hormone Resistant, Chemotherapy Naive Prostate Cancer
NCT01313559 · Sidney Kimmel Comprehensive Cancer Center at Thomas Jefferson University
TerminatedPhase 22011-066
A Study in Healthy Subjects to Assess the Safety, Tolerability, PK and PD of HTL0030310
NCT03847207 · Nxera Pharma UK Limited
CompletedPhase 12019-01-2342
Pasireotide as Maintenance Treatment in Synovial Sarcoma and Desmoplastic Small Round Cell Tumor
NCT06456359 · University Hospital Heidelberg
RecruitingPhase 22024-12-1928
Long Term Safety and Efficacy of Pasireotide s.c. in Patients With Cushing's Disease
NCT02310269 · RECORDATI GROUP
Completed2013-03-28152
Study to Allow Access to Pasireotide for Patients Benefiting From Pasireotide Treatment in Novartis-sponsored Studies
NCT01794793 · RECORDATI GROUP
CompletedPhase 42013-06-10337
The RApid Switch From 1st Generation Somatostatin Analogues to PaSireOtiDe In Acromegaly
NCT06597383 · IRCCS San Raffaele
Status unknown2023-11-24100
Pasireotide to Reduce Clinically Relevant Digestive Leakage After Complete Cytoreductive Surgery (CRS) Plus Hyperthermic Intra-Peritoneal Chemotherapy (HIPEC) for Peritoneal Carcinomatosis
NCT04826432 · Gustave Roussy, Cancer Campus, Grand Paris
TerminatedPhase 22020-09-036
Study of Pasireotide Long Acting Release (LAR) in Patients With Metastatic Neuroendocrine Tumors (NETs)
NCT01253161 · H. Lee Moffitt Cancer Center and Research Institute
CompletedPhase 22011-02-0129
Compassionate Use of SOM230 for Hyperinsulinemic/Hypoglycemia
NCT02835131 · Montefiore Medical Center
NO_LONGER_AVAILABLE

Exenatide

StudyStatusPhaseStartPeople
A Pan-European Post-Authorisation Safety Study: Risk of Pancreatic Cancer Among Type 2 Diabetes Patients Who Initiated Exenatide as Compared With Those Who Initiated Other Non-Glucagon-Like Peptide 1 Receptor Agonists Based Glucose Lowering Drugs
NCT05663515 · AstraZeneca
Recruiting2024-09-3024000
Efficacy and Safety of Exenatide in the Treatment of Hypothalamic Obesity After Craniopharyngioma Therapy
NCT02860923 · University Hospital, Bordeaux
CompletedPhase 32017-01-1142
Effect of GLP-1 Receptor (GLP-1R) Agonists on Cardiac Function and on Epicardial Adipose Tissue (EAT) Volume and on Myocardial TG Content in Obese Diabetics
NCT02042664 · Assistance Publique Hopitaux De Marseille
CompletedPhase 32011-0144
Exenatide Once Weekly Over 2 Years as a Potential Disease Modifying Treatment for Parkinson's Disease
NCT04232969 · University College, London
CompletedPhase 32020-01-20194
Exenatide Pharmacokinetics and Pharmacodynamics in Gestational Diabetes
NCT05482789 · Maisa N. Feghali, MD
RecruitingPhase 42023-04-1213
A Single-Center, Open-Label, Single Ascending Dose Study of Exenatide Circular RNA-Lipid Nanoparticle Injection (CR059) in Chinese Subjects With Type 2 Diabetes Mellitus
NCT07347080 · The First Affiliated Hospital of Henan University of Science and Technology
RecruitingEarly phase 12026-01-209
Exenatide for Smoking Cessation and Prevention of Weight Gain
NCT05610800 · The University of Texas Health Science Center, Houston
CompletedPhase 22022-12-07140
Exenatide For Reducing the Reinforcing Effects of Cocaine
NCT06252623 · Christopher D. Verrico
WithdrawnPhase 12024-08-010
Extended Release Exenatide Versus Placebo In Diabetic Patients With Type 4 Cardiorenal Syndrome
NCT02251431 · Baylor Research Institute
CompletedPhase 32015-1157
Identification and Clinical Relevance of an Oxytocin Deficient State (GLP1 Study)
NCT04897802 · Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
CompletedPhase 42021-09-1342
Diabetes Islet Preservation Immune Treatment
NCT02586831 · Camillo Ricordi and Jay Skyler
WithdrawnPhase 1 / Phase 22024-06-010
Brain Activation and Satiety in Children 2
NCT04520490 · Seattle Children's Hospital
Active, not recruitingPhase 32021-01-2863
Comparison of Type 2 Diabetes Pharmacotherapy Regimens
NCT05073692 · Kaiser Permanente
Completed2021-07-01241981
Assessment of Safety, Tolerability and Drug Levels of Exenatide Implant
NCT05670379 · Vivani Medical, Inc
CompletedPhase 12024-12-2024
Association of Gene Polymorphism With Susceptibility to T2DM and the Therapeutic Responses to Exenatide in Chinese Patients With T2DM
NCT06256419 · The Affiliated Hospital of Xuzhou Medical University
RecruitingNot applicable2024-01-01300

Ghrelin

StudyStatusPhaseStartPeople
Effects of Different Exercise Types on Irisin, Leptin, and Ghrelin Levels in Sedentary Women
NCT07805772 · Inonu University
Not yet recruitingNot applicable2026-09-0520
Salivary Apelin, Chemerin, Ghrelin, and Lipocalin-2 Levels in Diabetic Patients With Periodontitis
NCT07703345 · Necmettin Erbakan University
Recruiting2026-07-0188
Circulating Ghrelin as a Biomarker for Dementia
NCT05381090 · Swansea University
CompletedNot applicable2022-08-1585
Ghrelin and Nutritional Status After a Standardized Meal.
NCT07627802 · Medical University of Bialystok
CompletedNot applicable2025-04-0880
Unacylated Ghrelin to Improve Functioning in PAD
NCT04377126 · Northwestern University
CompletedPhase 22020-07-0825
Effects of Antagonizing the Ghrelin Receptor on Brain Food Cue Reactivity in Obesity
NCT06845033 · University Hospital, Gentofte, Copenhagen
Active, not recruitingNot applicable2025-05-0128
Functional Proteins in Polycystic Ovary Syndrome
NCT06793098 · Jagiellonian University
Recruiting2025-01-20100
Validation of the Concept of the Autoantibodies Directed Against the Neuropeptides Involved in Food Intake Regulation on the Incidental Cases of Eating Disorders
NCT03510533 · University Hospital, Rouen
CompletedNot applicable2018-05-24211
Effects of Ghrelin Administration on Motivation
NCT06576440 · University Hospital Tuebingen
CompletedNot applicable2024-09-0224
Effects of Ghrelin Administration on Dopamine and Effort
NCT05318924 · University Hospital Tuebingen
CompletedPhase 1 / Phase 22022-02-2126
Effects of Obesity and Intensity of Exercise on Ghrelin Levels
NCT04581980 · University of Virginia
CompletedNot applicable2020-10-1440
Co-Feedback Action of Growth Hormone, PP and PYY on Ghrelin in Bulimia
NCT03338387 · Charles University, Czech Republic
Enrolling by invitationPhase 22003-05-0624
Dialectical Behavioral Therapy As A Therapeutic Tool In Patients With Binge Eating Disorder
NCT05560529 · Alexandria University
CompletedPhase 42023-03-1560
Manipulating Ghrelin Signaling Via GOAT Inhibition in Alcohol Use Disorder
NCT03896516 · National Institute on Drug Abuse (NIDA)
CompletedPhase 1 / Phase 22021-06-2221
Translational and Clinical Aspects of Metabolic, Anabolic and Endothelial Dysfunction in Heart Failure
NCT05277415 · Lars Lund
CompletedPhase 1 / Phase 22013-02-1731

Kisspeptin-10

StudyStatusPhaseStartPeople
Prolonged Pulsatile Kisspeptin Administration in Hypogonadotropic Hypogonadism
NCT04648969 · Stephanie B. Seminara, MD
CompletedPhase 22019-05-0318
Kisspeptin Administration Subcutaneously to Patients With IHH
NCT05896293 · Stephanie B. Seminara, MD
RecruitingPhase 22023-02-0336
Kisspeptin Administration Subcutaneously to Patients With Hypothalamic Amenorrhea
NCT07224438 · Stephanie B. Seminara, MD
RecruitingPhase 22025-12-0920
Kisspeptin to Quantify GnRH Neuronal Function in Health and Disease
NCT07224490 · Stephanie B. Seminara, MD
RecruitingPhase 12026-03-1040
Functional Proteins in Polycystic Ovary Syndrome
NCT06793098 · Jagiellonian University
Recruiting2025-01-20100
Recall by Genotype: Neuropeptide Stimulation
NCT05901467 · Stephanie B. Seminara, MD
TerminatedPhase 12023-10-2016
Evaluation of Kisspeptin Glucose-Stimulated Insulin Secretion With Oral Glucose Tolerance Test
NCT04958109 · Massachusetts General Hospital
CompletedPhase 12021-10-2816
Dampening the Reproductive Axis With Continuous Kisspeptin
NCT05971849 · Stephanie B. Seminara, MD
CompletedPhase 12023-10-068
Kisspeptin Administration Subcutaneously to Patients With Reproductive Disorders
NCT05633966 · Stephanie B. Seminara, MD
CompletedPhase 12022-12-1613
Administration of Kisspeptin in Patients With Hyperprolactinemia
NCT02956447 · Massachusetts General Hospital
CompletedPhase 22017-11-1736
Reproductive Hormones During Sustained Administration of Kisspeptin
NCT02081924 · Imperial College London
RecruitingNot applicable2014-04-0276
A Prospective Cohort Study on the Serum Kisspeptin Levels Throughout Pregnancy in PCOS
NCT06545994 · Fudan University
Status unknown2024-06-28180
Evaluation of Kisspeptin Stimulated Insulin Secretion With Hyperglycemic Clamp
NCT05456854 · Massachusetts General Hospital
WithdrawnPhase 12022-06-030
Evaluation of Kisspeptin Glucose-Stimulated Insulin Secretion With Physiologic Mixed Meal Tolerance
NCT04532801 · Stephanie B. Seminara, MD
WithdrawnPhase 12019-09-010
Neuropeptides in Human Reproduction
NCT01952782 · Massachusetts General Hospital
CompletedPhase 12014-04-3061

Kisspeptin-54

StudyStatusPhaseStartPeople
Prolonged Pulsatile Kisspeptin Administration in Hypogonadotropic Hypogonadism
NCT04648969 · Stephanie B. Seminara, MD
CompletedPhase 22019-05-0318
Kisspeptin Administration Subcutaneously to Patients With IHH
NCT05896293 · Stephanie B. Seminara, MD
RecruitingPhase 22023-02-0336
Kisspeptin Administration Subcutaneously to Patients With Hypothalamic Amenorrhea
NCT07224438 · Stephanie B. Seminara, MD
RecruitingPhase 22025-12-0920
Kisspeptin to Quantify GnRH Neuronal Function in Health and Disease
NCT07224490 · Stephanie B. Seminara, MD
RecruitingPhase 12026-03-1040
Functional Proteins in Polycystic Ovary Syndrome
NCT06793098 · Jagiellonian University
Recruiting2025-01-20100
Recall by Genotype: Neuropeptide Stimulation
NCT05901467 · Stephanie B. Seminara, MD
TerminatedPhase 12023-10-2016
Evaluation of Kisspeptin Glucose-Stimulated Insulin Secretion With Oral Glucose Tolerance Test
NCT04958109 · Massachusetts General Hospital
CompletedPhase 12021-10-2816
Dampening the Reproductive Axis With Continuous Kisspeptin
NCT05971849 · Stephanie B. Seminara, MD
CompletedPhase 12023-10-068
Kisspeptin Administration Subcutaneously to Patients With Reproductive Disorders
NCT05633966 · Stephanie B. Seminara, MD
CompletedPhase 12022-12-1613
Administration of Kisspeptin in Patients With Hyperprolactinemia
NCT02956447 · Massachusetts General Hospital
CompletedPhase 22017-11-1736
Reproductive Hormones During Sustained Administration of Kisspeptin
NCT02081924 · Imperial College London
RecruitingNot applicable2014-04-0276
A Prospective Cohort Study on the Serum Kisspeptin Levels Throughout Pregnancy in PCOS
NCT06545994 · Fudan University
Status unknown2024-06-28180
Evaluation of Kisspeptin Stimulated Insulin Secretion With Hyperglycemic Clamp
NCT05456854 · Massachusetts General Hospital
WithdrawnPhase 12022-06-030
Evaluation of Kisspeptin Glucose-Stimulated Insulin Secretion With Physiologic Mixed Meal Tolerance
NCT04532801 · Stephanie B. Seminara, MD
WithdrawnPhase 12019-09-010
Neuropeptides in Human Reproduction
NCT01952782 · Massachusetts General Hospital
CompletedPhase 12014-04-3061

Setmelanotide

StudyStatusPhaseStartPeople
A Trial of Setmelanotide in Acquired Hypothalamic Obesity
NCT05774756 · Rhythm Pharmaceuticals, Inc.
Active, not recruitingPhase 32023-04-26143
EMANATE: A Study of Setmelanotide in Patients With Specific Gene Variants in the MC4R Pathway
NCT05093634 · Rhythm Pharmaceuticals, Inc.
CompletedPhase 32021-12-10296
Setmelanotide to Treat Obesity in a Patient With Pseudohypoparathyroidism Type 1a (PHP1a)
NCT07496463 · Massachusetts General Hospital
Enrolling by invitationPhase 22026-07-211
Open-Label Extension Study of Setmelanotide
NCT06596135 · Rhythm Pharmaceuticals, Inc.
CompletedPhase 32024-10-2128
Real-World Effects of MC4R Agonist Therapy in BBS and Severe Genetic Obesity
NCT07674290 · Tom Hühne
RecruitingPhase 42023-01-01200
A Study of Setmelanotide in Patients With Prader-Willi Syndrome
NCT06772597 · Rhythm Pharmaceuticals, Inc.
Active, not recruitingPhase 22025-03-0418
A Trial of Setmelanotide in Patients With Congenital Hypothalamic Obesity (Sub-study of NCT05774756)
NCT06760546 · Rhythm Pharmaceuticals, Inc.
RecruitingPhase 32025-09-2339
DAYBREAK: A Study of Setmelanotide in Participants With Specific Gene Variants in the Melanocortin-4 Receptor (MC4R) Pathway
NCT04963231 · Rhythm Pharmaceuticals, Inc.
CompletedPhase 22021-11-30164
Long Term Extension Trial of Setmelanotide
NCT03651765 · Rhythm Pharmaceuticals, Inc.
CompletedPhase 2 / Phase 32018-07-15205
Open-Label Study of Setmelanotide in Hypothalamic Obesity
NCT04725240 · Rhythm Pharmaceuticals, Inc.
CompletedPhase 22021-06-0718
Setmelanotide in Pediatric Participants With Rare Genetic Diseases of Obesity
NCT04966741 · Rhythm Pharmaceuticals, Inc.
CompletedPhase 32022-03-0812
Phase 3 Crossover Trial of Two Formulations of Setmelanotide in Participants With Specific Gene Defects in the MC4R Pathway
NCT05194124 · Rhythm Pharmaceuticals, Inc.
CompletedPhase 32021-12-2119
Study of Setmelanotide Effects on QTc (Corrected QT) Interval in Healthy Participants
NCT05046132 · Rhythm Pharmaceuticals, Inc.
CompletedPhase 42021-08-0577
Setmelanotide (RM-493), Melanocortin-4 Receptor (MC4R) Agonist, in Bardet-Biedl Syndrome (BBS) and Alström Syndrome (AS) Participants With Moderate to Severe Obesity
NCT03746522 · Rhythm Pharmaceuticals, Inc.
CompletedPhase 32018-11-2352
Setmelanotide for the Treatment of Early-Onset Pro-Opiomelanocortin (POMC) Deficiency Obesity
NCT02896192 · Rhythm Pharmaceuticals, Inc.
CompletedPhase 32017-02-1415

Lixisenatide

StudyStatusPhaseStartPeople
A Study to Investigate Safety and Efficacy of iGlarLixi in Adult Patients With Type 2 Diabetes Mellitus
NCT06716424 · Sanofi
CompletedPhase 42025-01-06105
Efficacy and Safety of iGlarLixi Versus Standard of Care in a Real-world Adult China Population With Uncontrolled Type 2 Diabetes on Oral Agents
NCT07307235 · Shanghai Zhongshan Hospital
RecruitingPhase 42025-12-131316
iGlarLixi CGM Study in Chinese T2D Individuals After OADs
NCT06671587 · Sanofi
RecruitingPhase 42024-12-10678
Regimen Transition After Short-Term Intensive Insulin Therapy in Type 2 Diabetes
NCT07173712 · Yanbing Li
Not yet recruitingPhase 42026-03-15324
Study to Evaluate the Effect of Lixisenatide in Patient With Parkinson's Disease
NCT03439943 · University Hospital, Toulouse
CompletedPhase 22018-06-13156
iGlarLixi vs IDegAsp in Chinese Participants After OAD(s)
NCT05413369 · Sanofi
CompletedPhase 32022-07-07582
Evaluation of the Efficacy and Safety of GLP-1 Receptor Agonist Therapy In Steroid-Induced Diabetes
NCT07117240 · Medical University of Warsaw
Enrolling by invitationPhase 42025-07-10100
Effect of Soliqua 100/33 on Time in Range From Continuous Glucose Monitoring in Insulin-naive Patients With Very Uncontrolled Type 2 Diabetes Mellitus
NCT05114590 · Sanofi
CompletedPhase 42022-01-27124
Lixisenatide-The Effects on Glucose and Lipid Metabolism in Type 2 Diabetes
NCT02049034 · University of Surrey
CompletedPhase 42014-018
The Effect of Lixisenatide on the Effect of Pituitary Hormones
NCT05804513 · University of Tartu
Status unknownPhase 42023-04-1710
Evaluation of Insulin Glargine/Lixisenatide Fixed Ratio Combination in Patients With Type 2 Diabetes Insufficiently Controlled With Oral Antidiabetic Drug(s)
NCT03798054 · Sanofi
CompletedPhase 32019-02-15878
Comparison of the Efficacy and Safety of Insulin Glargine/Lixisenatide Fixed Ratio Combination to Insulin Glargine in Patients With Type 2 Diabetes Insufficiently Controlled on Basal Insulin
NCT03798080 · Sanofi
CompletedPhase 32019-02-19426
Study Comparing the Efficacy and Safety of Insulin Glargine (Basal Insulin)/Lixisenatide (GLP-1 Receptor Agonist) Combination (Soliqua™) in Patients With Type 2 Diabetes Mellitus (T2DM)
NCT03767543 · Sanofi
CompletedPhase 32019-03-11265
A Study on Safety, Pharmacokinetics and Pharmacodynamics of Lixisenatide in Pediatric Patients With Type 2 Diabetes Mellitus (T2DM)
NCT02803918 · Sanofi
CompletedPhase 12017-05-1723
Safety Assessment of Lyxumia (Lixisenatide) and Sulfonylurea as Add-on Treatment to Basal Insulin in Uncontrolled Patients With Type 2 Diabetes Mellitus Who Elect to Fast During Ramadan
NCT02941367 · Sanofi
CompletedPhase 42017-02-23184

Teduglutide

StudyStatusPhaseStartPeople
A Survey to Assess Participants' and Physicians' Knowledge When Using GATTEX (Knowledge Assessment Survey)
NCT05561647 · Takeda
Completed2013-08-01600
A Study of Teduglutide in Chinese Adults With Short Bowel Syndrome
NCT06973304 · Takeda
Active, not recruitingPhase 32025-06-2613
A Study of Teduglutide in Japanese People With Short Bowel Syndrome
NCT05023382 · Takeda
Completed2021-09-01250
Glucagon-like Peptide 2 (GLP-2) in Undernourished Women Improving From Histology-Confirmed Environmental Enteric Dysfunction (EED)
NCT07537686 · International Centre for Diarrhoeal Disease Research, Bangladesh
Not yet recruitingPhase 22026-07-0155
A Study of Teduglutide in Chinese Children and Teenagers With Short Bowel Syndrome
NCT07319832 · Takeda
Recruiting2026-03-0512
TED_ORG: Study on Short Bowel Syndrome
NCT07400783 · Meyer Children's Hospital IRCCS
RecruitingNot applicable2024-10-3050
Characterization of the Long-term Safety, Efficacy, and Pharmacodynamics Revestive® in the Management of Short Bowel Syndrome Pediatric Patients
NCT03562130 · Assistance Publique - Hôpitaux de Paris
CompletedPhase 42018-07-0225
A Study of Teduglutide (Revestive®) in Participants With Short Bowel Syndrome (SBS) in Canada
NCT05371028 · Takeda
Completed2023-09-2352
Long-term Safety and Efficacy Study of Teduglutide in Pediatric Participants With Short Bowel Syndrome (SBS)
NCT02954458 · Shire
CompletedPhase 32017-01-0961
Long-term Study of Teduglutide in Pediatric Subjects With Short Bowel Syndrome Who Completed the TED-C13-003 Study
NCT02949362 · Shire
CompletedPhase 32016-12-0929
A Study of Teduglutide in Japanese Children With Short Bowel Syndrome Aged 4 Months or Older
NCT05027308 · Takeda
CompletedPhase 32022-01-043
Pediatric Teduglutide Registry
NCT04832087 · Boston Children's Hospital
Completed2021-05-18142
Treatment of Patients With Teduglutide (GLP-2) for GVHD and Analysis of Paneth Cells of GVHD Patients
NCT04290429 · University of Freiburg
CompletedEarly phase 12017-12-066
A Study With Teduglutide (Revestive®) in Adults With Short Bowl Syndrome
NCT04883606 · Takeda
Completed2022-01-2665
A Study of Teduglutide (Revestive®) in Children, Teenagers and Adults With Short Bowel Disease
NCT04877431 · Takeda
Completed2020-11-0545

NAD+

StudyStatusPhaseStartPeople
PEDIatric Cardiac Dysfunction Treated With Injectable Nicotinamide Adenine Dinucleotide
NCT07839130 · Beijing Children's Hospital
Not yet recruitingPhase 22026-10-01180
A Clinical Trial to Assess the Absorption, Safety, and Efficacy of an Oral Nicotinamide Adenine Dinucleotide (NAD+) Supplement in Healthy Adults
NCT07692633 · Reus Research
Not yet recruitingNot applicable2026-0880
Nicotinamide Adenine Dinucleotide Responses to a Nutritional Supplement
NCT07428889 · Shaklee Corporation
CompletedNot applicable2026-02-1729
Nicotinamide Adenine Dinucleotide (NAD+) Metabolism in Human Brown Adipose Tissue
NCT06627868 · University of Turku
RecruitingNot applicable2024-11-2068
NADream: Effects of Nicotinamide Adenine Dinucleotide Supplementation on Sleep Quality in Healthy Individuals
NCT06971224 · Haukeland University Hospital
RecruitingPhase 22025-10-1316

Pramlintide

StudyStatusPhaseStartPeople
Postprandial Regulation of Bone Perfusion in Healthy Individuals
NCT07679516 · University of Copenhagen
Not yet recruitingNot applicable2026-07-1915
Two Way Crossover Closed Loop Study Insulin vs Insulin and Pramlintide
NCT06422325 · Oregon Health and Science University
CompletedNot applicable2024-07-1233
Multi-Center Development of a Novel Diagnostic Test for Alzheimer's Disease
NCT03560960 · Boston University
Active, not recruitingEarly phase 12020-02-0457
Tailoring Obesity Treatment Trial
NCT06619015 · Esbjerg Hospital - University Hospital of Southern Denmark
WithdrawnPhase 2 / Phase 32025-04-010
Pancreatic Polypeptide as a Modulator of Amylin- Induced Satiety in Healthy Humans
NCT07506369 · University Hospital, Gentofte, Copenhagen
RecruitingNot applicable2026-0418
A Fully Automated Lyumjev and Pramlintide Delivery System for Adults With Type 1 Diabetes
NCT06046417 · McGill University Health Centre/Research Institute of the McGill University Health Centre
Status unknownPhase 2 / Phase 32023-11-3030
Phase 2, Randomized, Open-Label, Crossover, PD/PK Study of a Novel Pram-Insulin Co-Formulation in Adults With T1D
NCT04074317 · Xeris Pharmaceuticals
CompletedPhase 22019-08-2218
The Role of Amylin in Bone Metabolism
NCT06186063 · Filip Krag Knop
Status unknownNot applicable2024-02-1220
A Fully-closed Loop, Pramlintide and Insulin, Artificial Pancreas Clinical Trial for Adults With Type 1 Diabetes
NCT05199714 · McGill University Health Centre/Research Institute of the McGill University Health Centre
CompletedNot applicable2022-02-2112
Pramlintide (Symlin) for the Treatment of Hypoglycemia Following Gastric Bypass Surgery
NCT01841359 · Joslin Diabetes Center
CompletedPhase 42010-02-0222
Biological Outcomes of Pramlintide in Resectable Cutaneous Squamous Cell Carcinoma: A Pilot Study
NCT04252612 · H. Lee Moffitt Cancer Center and Research Institute
WithdrawnEarly phase 12020-01-300
Co-administration of Pramlintide and Insulin Via an Automated Dual-hormone Artificial Pancreas System in Adults With Type 1 Diabetes
NCT04243629 · McGill University
Status unknownNot applicable2021-11-1226
A Study of the Functional Magnetic Resonance Imaging Response to Leptin and Pramlintide
NCT00691158 · Oregon Health and Science University
Status unknownNot applicable2006-0110
Alleviating Carbohydrate Counting for Patients With Type 1 Diabetes Using a Novel Insulin-plus-pramlintide Artificial Pancreas
NCT04163874 · McGill University
CompletedNot applicable2020-02-1436
Glucagon Counterregulation in Type 1 Diabetes
NCT03547427 · University of Virginia
TerminatedNot applicable2018-05-2013

Elamipretide

StudyStatusPhaseStartPeople
ReNEW:Phase 3 Study of Efficacy, Safety & Pharmacokinetics of Subcutaneous Injections of Elamipretide in Subjects With Dry Age-Related Macular Degeneration (Dry AMD)
NCT06373731 · Stealth BioTherapeutics Inc.
Active, not recruitingPhase 32024-05-30313
Clinical Trial in Patients With Barth Syndrome- 4TAZPower
NCT07531251 · Stealth BioTherapeutics Inc.
RecruitingPhase 42026-07-0248
FRDA Investigator Initiated Study (IIS) With Elamipretide
NCT05168774 · Children's Hospital of Philadelphia
CompletedPhase 1 / Phase 22022-03-0320
Study of Healthy Aging and Physical Function With Elamipretide
NCT07275424 · David Marcinek
RecruitingPhase 22025-11-2630
Study to Evaluate Efficacy and Safety of Elamipretide in Subjects With Primary Mitochondrial Disease From Nuclear DNA Mutations (nPMD)
NCT05162768 · Stealth BioTherapeutics Inc.
CompletedPhase 32022-04-29102
An Intermediate Size Expanded Access Protocol of Elamipretide
NCT04689360 · Stealth BioTherapeutics Inc.
AVAILABLE
ReCLAIM-2 Study to Evaluate Safety,Efficacy & Pharmacokinetics of Elamipretide in Subjects With AMD With Non-central GA
NCT03891875 · Stealth BioTherapeutics Inc.
CompletedPhase 22019-03-27176
A Trial to Evaluate Safety, Tolerability and Efficacy of Elamipretide in Subjects With Barth Syndrome
NCT03098797 · Stealth BioTherapeutics Inc.
CompletedPhase 2 / Phase 32017-07-0512
A Trial to Evaluate Safety and Efficacy of Elamipretide Primary Mitochondrial Myopathy Followed by Open-Label Extension
NCT03323749 · Stealth BioTherapeutics Inc.
TerminatedPhase 32017-10-09218
Open-Label Extension Trial to Characterize the Long-term Safety and Tolerability of Elamipretide in Subjects With Genetically Confirmed Primary Mitochondrial Myopathy (PMM)
NCT02976038 · Stealth BioTherapeutics Inc.
TerminatedPhase 22016-1228
A Study Investigating the Safety, Tolerability, and Efficacy of Elamipretide Topical Ophthalmic Solution for Treatment of Leber's Hereditary Optic Neuropathy
NCT02693119 · Stealth BioTherapeutics Inc.
CompletedPhase 22016-0312
A Study Investigating the Safety, Tolerability, and Efficacy of Elamipretide Topical Ophthalmic Solution for the Treatment of Fuchs' Corneal Endothelial Dystrophy (FCED)
NCT02653391 · Stealth BioTherapeutics Inc.
CompletedPhase 1 / Phase 22016-0222
An Open-Label, Phase 1 Clinical Study to Evaluate the Safety and Tolerability of Subcutaneous Elamipretide in Subjects With Intermediate Age-Related Macular Degeneration
NCT02848313 · Stealth BioTherapeutics Inc.
CompletedPhase 12016-10-2840
A Phase 2 Study to Evaluate the Cardiac and Renal Effects of Short Term Treatment With Elamipretide in Patients Hospitalized With Congestion Due to Heart Failure
NCT02914665 · Stealth BioTherapeutics Inc.
CompletedPhase 22016-10-20308
Safety, Tolerability, Efficacy of MTP-131 for Treatment of Mitochondrial Disease in Subjects From the MMPOWER Study
NCT02805790 · Stealth BioTherapeutics Inc.
CompletedPhase 22016-08-2230

Thymosin beta-4

StudyStatusPhaseStartPeople
Assessment of the Safety and Efficacy of RGN-259 Ophthalmic Solutions for Dry Eye Syndrome: ARISE-3
NCT03937882 · ReGenTree, LLC
CompletedPhase 32019-05-24700
Recombinant Human Thymosin Beta 4 for Injection(NL005) for Acute Myocardial Infarction
NCT07586865 · Beijing Northland Biotech. Co., Ltd.
Not yet recruitingPhase 22026-05-18189
TB-500 (Thymosin Beta 4 17-23 Fragment) for Cardiovascular Biomarkers in Stable ASCVD
NCT07487363 · Hudson Biotech
RecruitingPhase 1 / Phase 22026-02-0580
Assessment of the Safety and Efficacy of 0.1% RGN-259 Ophthalmic Solution for the Treatment of NK: SEER-2
NCT05555589 · ReGenTree, LLC
RecruitingPhase 32023-04-1170
Efficacy and Safety Study of Thymosin Beta 4 in Patients With Acute Myocardial Infarction
NCT05984134 · Beijing Northland Biotech. Co., Ltd.
CompletedPhase 22022-07-1590
Assessment of the Safety and Efficacy Study of RGN-259 Ophthalmic Solutions for Neurotrophic Keratopathy : SEER-1
NCT02600429 · ReGenTree, LLC
TerminatedPhase 32015-09-1718
Safety and Efficacy Study of Thymosin Beta 4 in Patients With Acute Myocardial Infarction.Infarction
NCT05485818 · Beijing Northland Biotech. Co., Ltd.
CompletedPhase 22020-11-2362
Assessment of the Safety and Efficacy of RGN-259 Ophthalmic Solutions for Dry Eye Syndrome : ARISE-2
NCT02974907 · ReGenTree, LLC
CompletedPhase 32016-11601
A Study of the Safety and Efficacy of Injectable Thymosin Beta 4 for Treating Acute Myocardial Infarction
NCT01311518 · RegeneRx Biopharmaceuticals, Inc.
WithdrawnPhase 22019-070
A Phase 1a Study of Thymosin Beta 4 in Healthy Volunteers
NCT04555824 · Beijing Northland Biotech. Co., Ltd.
CompletedPhase 12017-07-1754
A Phase 1b Study of Thymosin Beta 4 in Healthy Volunteers
NCT04555850 · Beijing Northland Biotech. Co., Ltd.
CompletedPhase 12018-07-3030
Assessment of the Safety and Efficacy of RGN-259 Ophthalmic Solutions for Dry Eye Syndrome: ARISE-1
NCT02597803 · ReGenTree, LLC
CompletedPhase 2 / Phase 32015-09317
A Phase 1 Safety Study of the Intravenous Administration of Thymosin Beta in Healthy Volunteers
NCT00743769 · RegeneRx Biopharmaceuticals, Inc.
WithdrawnPhase 12008-040
Comparative Study of Thymosin Beta 4 Eye Drops vs. Vehicle in the Treatment of Severe Dry Eye
NCT01393132 · Michigan Cornea Consultants, PC
CompletedPhase 22011-039
Safety and Efficacy of Thymosin Beta 4 Ophthalmic Solution in Patients With Dry Eye
NCT01387347 · ReGenTree, LLC
CompletedPhase 22011-0872

Tesamorelin

StudyStatusPhaseStartPeople
Body Composition and Adipose Tissue in HIV
NCT03226821 · Columbia University
TerminatedPhase 42018-02-076
Tesamorelin as an Adjunct to Exercise for Improving Physical Function in HIV
NCT06554717 · Massachusetts General Hospital
RecruitingPhase 22025-07-10100
Tesamorelin for Reduction of Liver Fat in Adults With Fatty Liver Disease (Mock Study)
NCT07481734 · Hudson Biotech
RecruitingPhase 22026-02-02120
Phase II Trial of Tesamorelin for Cognition in Aging HIV-Infected Persons
NCT02572323 · University of California, San Diego
CompletedPhase 22017-02-1573
Growth Hormone Releasing Hormone Analog to Improve Nonalcoholic Fatty Liver Disease and Associated Cardiovascular Risk
NCT03375788 · Massachusetts General Hospital
CompletedPhase 22019-01-1751
Tesamorelin to Improve Functional Outcomes After Peripheral Nerve Injury
NCT03150511 · Johns Hopkins University
RecruitingPhase 22018-06-0136
TH9507 Extension Study in Patients With HIV-Associated Lipodystrophy
NCT00608023 · Theratechnologies
CompletedPhase 32007-08263
Efficacy and Safety Study of Tesamorelin in Chronic Obstructive Pulmonary Disease (COPD) Subjects With Muscle Wasting
NCT01388920 · Theratechnologies
TerminatedPhase 22011-093
Tesamorelin Effects on Liver Fat and Histology in HIV
NCT02196831 · Massachusetts General Hospital
CompletedNot applicable2015-07-0161
Impact of GHRH on Sleep Promotion and Endocrine Regulation in Service Members Who Sustained a Traumatic Brain Injury and Have Current Insomnia
NCT02931474 · National Institute of Nursing Research (NINR)
WithdrawnPhase 22016-10-060
Diabetic Retinopathy in HIV Subjects Treated With EGRIFTA®
NCT01591902 · Theratechnologies
TerminatedPhase 42012-06129
Long-term Observational Study in HIV Subjects Exposed to EGRIFTA®
NCT01579695 · Theratechnologies
Terminated2013-02391
Effects of Growth Hormone Releasing Hormone in HIV
NCT01263717 · Massachusetts General Hospital
CompletedNot applicable2010-1254
Egrifta Replacement and Sleep Disordered Breathing
NCT01788462 · Johns Hopkins University
Withdrawn2012-050
Abdominal Obesity, Cardiovascular Inflammation, and Effects of Growth Hormone Releasing Hormone Analogue
NCT01632592 · Massachusetts General Hospital
WithdrawnNot applicable2014-010

Ziconotide

StudyStatusPhaseStartPeople
Intrathecal Ziconotide in Chemotherapy Induced Peripheral Neuropathy
NCT07499882 · Christian Hospital Northeast Northwest
Not yet recruiting2026-05-0224
OP2C : Prialt® Observatory in Clinical Practice
NCT04321408 · Institut Cancerologie de l'Ouest
Recruiting2020-07-10300
Ziconotide for Non-cancer Pain by Intrathecal Administration
NCT06541184 · ESTEVE Pharmaceuticals SAS
Recruiting2024-10-3085
Safety and Activity Study of Intrathecally Administered Ziconotide for Neuropathic Pain in Patients With Cancer
NCT00996983 · National Cancer Institute, Naples
Status unknownPhase 22009-0916
Ziconotide as First-Line IDT
NCT03321955 · Albany Medical College
CompletedPhase 42016-11-0313
Intrathecal Ziconotide Antalgic Efficacy for Severe Refractory Neuropathic
NCT03942848 · Hospices Civils de Lyon
Status unknownPhase 32019-06-2044
Patient Registry of Intrathecal Pain Management in Europe for Prialt (Ziconotide Intrathecal Infusion) and Alternative Drugs for the Management of Severe, Chronic Pain.
NCT02268812 · Eisai Limited
Completed2008-04219
Single Shot Intrathecal Ziconotide for Painful Neuropathy or Myelopathy
NCT01992562 · Aaron Boster
WithdrawnPhase 42014-010
Patient Registry of Intrathecal Ziconotide Management(PRIZM)
NCT01888120 · Jazz Pharmaceuticals
Completed2013-0793
Prialt (Ziconotide) In Severe Chronic Pain
NCT00047749 · Elan Pharmaceuticals
CompletedPhase 32002-08220
Ziconotide Effectiveness and Safety Trial in Patients With Chronic Severe Pain
NCT00076544 · Elan Pharmaceuticals
CompletedPhase 32004-02300
Intrathecal Bolus Doses of Ziconotide
NCT01373983 · University Hospital, Linkoeping
CompletedPhase 42011-0826
A Multicenter Phase II/III, Placebo-Controlled Study of SNX-111 Administered Intrathecally to Cancer and AIDS Patients With Chronic Pain
NCT00002160 · Neurex
CompletedPhase 2100

Pemvidutide

StudyStatusPhaseStartPeople
Phase 3 Study of the Efficacy, Safety, and Clinical Outcomes of Pemvidutide in MASH
NCT07795164 · Altimmune, Inc.
RecruitingPhase 32026-07-301800
QUILT-2.008: Study of ALT-801 With Cisplatin in Patients With Metastatic Melanoma
NCT01029873 · Altor BioScience
TerminatedPhase 1 / Phase 22010-0222
RESTORE TRIAL: Study of the Efficacy and Safety of Pemvidutide in the Treatment of Alcohol-Associated Liver Disease (ALD)
NCT07009860 · Altimmune, Inc.
Active, not recruitingPhase 22025-06-16121
RECLAIM STUDY: Phase 2 Study of the Efficacy and Safety of Pemvidutide in the Treatment of Alcohol Use Disorder (AUD) in Subjects With Obesity or Overweight
NCT06987513 · Altimmune, Inc.
CompletedPhase 22025-05-15100
IMPACT TRIAL: Efficacy and Safety of Pemvidutide in Subjects With Nonalcoholic Steatohepatitis (NASH)
NCT05989711 · Altimmune, Inc.
CompletedPhase 22023-07-27212
ALT-801 in Overweight and Obese Subjects With Type 2 Diabetes Mellitus (T2DM)
NCT05134662 · Altimmune, Inc.
CompletedPhase 12022-02-0155
Pemvidutide (ALT-801) DDI Study in Healthy Volunteers
NCT04972396 · Altimmune, Inc.
CompletedPhase 12021-09-1540
ALT-801 (Pemvidutide) in Healthy Overweight and Obese Volunteers to Study Safety and Tolerability
NCT04561245 · Altimmune, Inc.
CompletedPhase 12020-11-10100
A Study of ALT-801 in Patients With Bacillus Calmette-Guerin (BCG) Failure Non-Muscle Invasive Bladder Cancer
NCT01625260 · Altor BioScience
TerminatedPhase 1 / Phase 22012-03-3012
A Study of ALT-801 in Combination With Cisplatin and Gemcitabine in Muscle Invasive or Metastatic Urothelial Cancer
NCT01326871 · Altor BioScience
CompletedPhase 1 / Phase 22011-09-0668
QUILT-3.020: A Study of ALT-801 in Patients With Relapsed or Refractory Multiple Myeloma
NCT01670994 · Altor BioScience
TerminatedPhase 1 / Phase 22012-08-146
Efficacy and Safety of ALT-801 in the Treatment of Obesity
NCT05295875 · Altimmune, Inc.
CompletedPhase 22022-03-31391
Extension of ALT-801 in Diabetic and Non-Diabetic Overweight and Obese Subjects With (NAFLD)
NCT05292911 · Altimmune, Inc.
CompletedPhase 12022-03-0964
ALT-801 in Diabetic and Non-Diabetic Overweight and Obese Subjects With Non-alcoholic Fatty Liver Disease (NAFLD)
NCT05006885 · Altimmune, Inc.
CompletedPhase 12021-09-3095
ALT-801-activated Natural Killer Cells After FLAG Induction for Acute Myeloid Leukemia
NCT01478074 · Altor BioScience
WithdrawnPhase 12011-110

PACAP-38

StudyStatusPhaseStartPeople
The Effect of Interventional Procedures on Serum CGRP and PACAP-38 Levels in Chronic Migraine
NCT07395908 · Aydin Adnan Menderes University
Active, not recruitingNot applicable2025-05-29100
Induction of Migraine Attacks With Aura Using Pituitary Adenylate Cyclase Activating Polypeptide-38
NCT07342296 · Danish Headache Center
Not yet recruitingNot applicable2026-02-0121
Migraine Induction Properties of PACAP-38 After Eptinezumab in Migraine Without Aura Patients.
NCT05635604 · Danish Headache Center
CompletedNot applicable2023-03-0138
Hypersensitivity to PACAP-38 in Post-Traumatic Headache
NCT05378061 · Danish Headache Center
Status unknownNot applicable2022-06-1621
The Hemodynamic Effects of PACAP38 After Glibenclamide Administration in Healthy Volunteers
NCT04960657 · Danish Headache Center
CompletedNot applicable2020-10-2022
PACAP38 Induced Headache, Migraine and Flushing in Patients With Migraine
NCT03881644 · Danish Headache Center
CompletedNot applicable2018-07-1737
PACAP38 Induced Headache and Rosacea-like Symptoms in Patients With Rosacea
NCT03878784 · Danish Headache Center
CompletedNot applicable2018-11-1238
The Role of Inflammation and Vasodilatation in PACAP38-induced Headache Using MRI on Healthy Subjects
NCT03585894 · Danish Headache Center
CompletedNot applicable2018-08-0134
To Evaluate the Blockade of CGRP in Preventing PACAP-38 Induced Migraine-like Attacks With AMG 334 in Migraine Patients
NCT02542605 · Amgen
CompletedPhase 12015-11-1135
PACAP-38 Infusion in Patients With Cluster Headache
NCT03814226 · Danish Headache Center
Status unknownNot applicable2018-01-0145
The Effect of Histamine H1 Receptor Antagonist, Clemastin, on PACAP38 Induced Headache in Migraine Patients
NCT02364453 · Song Guo
CompletedNot applicable2015-0220
Effect of PACAP38/VIP on Migraineurs Measured by Magnetic Resonance
NCT01471990 · Glostrup University Hospital, Copenhagen
CompletedNot applicable2011-0524
PACAP38´s (Pituitary Adenylate Cyclase-Activating Polypeptide) Headache Inducing Characteristics and Effects on the Cerebral Blood Flow
NCT00380263 · Danish Headache Center
CompletedNot applicable2006-1112

MOTS-c

StudyStatusPhaseStartPeople
Comparison of the Effects of General Anesthesia and Combined Spinal-Epidural Anesthesia on Ferroptosis, Humanin and MOTS-c Levels in Renal Transplantation
NCT07678073 · University of Gaziantep
RecruitingNot applicable2026-03-0168
MOTS-c for Improving Insulin Sensitivity in Adults With Prediabetes and Overweight/Obesity
NCT07505745 · Hudson Biotech
RecruitingPhase 22026-02-02120
Platelet Reactivity, B-amyloid, MOTS-c and Mortality of Type II Diabetics With CAD
NCT04027712 · University of Athens
Status unknown2014-01-01120

BPC-157

StudyStatusPhaseStartPeople
Impact of BPC-157 on Recovery Following Rotator Cuff Repair Surgery
NCT07803250 · University of Arkansas
Not yet recruitingPhase 12027-01-0130
BPC 157 for Acute Hamstring Muscle Strain Repair
NCT07437547 · Hudson Biotech
RecruitingPhase 22026-02-02120

GHK-Cu

StudyStatusPhaseStartPeople
Two-Part Study of the Effects of the X39 Patch on Circulating GHK and GHK-Cu Levels in Healthy Adults
NCT07706361 · LifeWave, Inc.
Not yet recruitingNot applicable2027-01100
Topical GHK-Cu Gel for Acute Skin Wound Healing
NCT07437586 · Hudson Biotech
RecruitingPhase 22026-02-0260

L-Carnosine

StudyStatusPhaseStartPeople
Polaprezinc (Zinc L-carnosine) in Infants With Gastroesophageal Reflux
NCT06678997 · University of Roma La Sapienza
CompletedNot applicable2024-12-0160
Nucleophilic Defense Against PM Toxicity (NEAT Trial)
NCT03314987 · University of Louisville
CompletedNot applicable2018-04-01299
Effects of Carnosine In Patients With Peripheral Arterial Disease Patients
NCT06480760 · Shahid Baba
RecruitingPhase 1 / Phase 22025-05-20144
Molecular Mediators of Physical Exercise and Carnosine Induced Effects in Patients With Preclinical and Early Stage Neurodegenerative Disease
NCT03330470 · Slovak Academy of Sciences
CompletedNot applicable2017-01-0126
Effect of Multi-ingredient on Visceral Adiposity & Non-alcoholic Fatty Liver Disease in Postmenopausal Women With Abdominal Obesity
NCT06377631 · Fundació Eurecat
CompletedNot applicable2024-06-0750
Carnosine for Peripheral Arterial Disease Patients
NCT05371145 · Shahid Baba
Status unknownPhase 1 / Phase 22023-03-0120
Effect of a Multi-ingredient on Visceral Adiposity and Non-alcoholic Fatty Liver Disease in Individuals With Abdominal Obesity
NCT05807204 · Fundació Eurecat
CompletedNot applicable2023-05-0120
Effect of Zinc Carnosine on Intestinal Permeability in Healthy Volunteers
NCT00149149 · Imperial College London
CompletedPhase 12005-05-0110
Carnosine Supplementation and Cardiovascular Function
NCT05723939 · Josip Juraj Strossmayer University of Osijek
Status unknownNot applicable2022-09-01100
Carnosine and Cognitive Training in Schizophrenia
NCT02686697 · Abraham Reichenberg
CompletedPhase 2 / Phase 32015-12-0160
Carnosine for Peripheral Arterial Disease
NCT04870229 · University of Louisville
CompletedPhase 22016-05-1210
Role of Carnosine in Combination With Vitamin B Complex in Preventing the Progression of Diabetic Neuropathy in Type 2 Diabetes Patients
NCT05422352 · Beni-Suef University
CompletedNot applicable2021-01-1460
The Potential of Carnosine Supplementation in Optimising Cardiometabolic Health
NCT02917928 · Monash University
Status unknownPhase 22016-1040
Carnosine Supplementation on Quantity/Quality of Oral Salivae.
NCT04295525 · University of Milan
Status unknownNot applicable2022-09-0160
Research on Prevention, Intervention and Mechanisms of Obesity and Its Comorbidities
NCT05211817 · Slovak Academy of Sciences
Status unknownNot applicable2021-11-0160

Afamelanotide

StudyStatusPhaseStartPeople
Pharmacokinetics of Afamelanotide in Erythropoietic Protoporphyria Patients
NCT06388642 · Clinuvel Europe Limited
CompletedPhase 1 / Phase 22024-03-0728
A Study to Compare the Efficacy and Safety of SCENESSE and Narrow-Band Ultraviolet (NB-UVB) Light Versus NB-UVB Light Alone in Patients With Vitiligo
NCT06109649 · Clinuvel, Inc.
Active, not recruitingPhase 32023-10-11200
Study to Evaluate the Safety and Efficacy of Afamelanotide in Patients With Variegate Porphyria (VP)
NCT05854784 · Clinuvel Pharmaceuticals Limited
CompletedPhase 22023-03-286
Afamelanotide and Narrow-Band Ultraviolet B (NB-UVB) Phototherapy in the Treatment of Nonsegmental Vitiligo (NSV)
NCT04525157 · Clinuvel Pharmaceuticals Limited
CompletedPhase 22014-06-0621
A Study to Evaluate the Safety and Efficacy of Afamelanotide in Patients With Xeroderma Pigmentosum C and V
NCT05370235 · Clinuvel Europe Limited
Status unknownPhase 22022-03-286
A Study to Evaluate the Safety and Efficacy of Afamelanotide in Patients With Xeroderma Pigmentosum (XP)
NCT05159752 · Clinuvel Europe Limited
Status unknownPhase 22021-10-196
A Proof of Concept Study to Evaluate the Safety of Afamelanotide in Patients With Acute Arterial Ischaemic Stroke (AIS)
NCT04962503 · Clinuvel Pharmaceuticals Limited
CompletedPhase 22021-06-036
DNA Repair Capacity of Afamelanotide on Ultraviolet Radiation-induced DNA Damage in Healthy Volunteers
NCT05368857 · Clinuvel (UK) Ltd.
CompletedPhase 12022-01-1910
A Study to Assess the Changes in Pigmentation and Safety of Afamelanotide in Patients With Vitiligo on the Face
NCT05210582 · Clinuvel, Inc.
Status unknownPhase 22022-10-116
Afamelanotide in Patients Suffering With Acne Vulgaris
NCT04943159 · Clinuvel Pharmaceuticals Limited
CompletedPhase 22010-08-243
Phase III Confirmatory Study in Erythropoietic Protoporphyria (EPP)
NCT00979745 · Clinuvel Pharmaceuticals Limited
CompletedPhase 32009-0974
Afamelanotide as Adjunctive Therapy in Patients Undergoing Photodynamic Therapy (PDT) Utilising Porfimer Sodium
NCT04425746 · Clinuvel Pharmaceuticals Limited
CompletedPhase 22008-08-0516
Afamelanotide in Patients Suffering From Polymorphic Light Eruption (PLE)
NCT04704713 · Clinuvel Pharmaceuticals Limited
CompletedPhase 32010-05-0531
A Safety Extension Study in Patients With Erythropoietic Protoporphyria (EPP)
NCT04578496 · Clinuvel Pharmaceuticals Limited
CompletedPhase 32011-07-1116
Phase II Confirmatory Study in Erythropoietic Protoporphyria (EPP)
NCT01097044 · Clinuvel Pharmaceuticals Limited
CompletedPhase 22010-0477

LL-37

StudyStatusPhaseStartPeople
Evaluation of 25(OH)D3 and LL-37 Levels in Periimplant Sulcus Fluid
NCT07280754 · Recep Tayyip Erdogan University
Not yet recruiting2025-12-3072
Peri-implant Vitamin D and Cathelicidin (LL-37) Levels
NCT06867250 · Altinbas University
Completed2021-04-0133
Association of Cathelicidin and Vitamin D Levels With the Category and Course of COPD
NCT05431218 · Karaganda Medical University
CompletedPhase 42020-02-18120
Cathelicidin LL-37 Relation to Potentially Malignant Lesions
NCT06219330 · Fayoum University
Completed2023-07-0145
The Role of Anti-inflammatory Cytokines and Antimicrobial Peptide LL-37 Biomarkers in the Treatment of Periodontal Disease.
NCT04404335 · Universidad Rey Juan Carlos
Completed2021-05-1760
Intratumoral Injections of LL37 for Melanoma
NCT02225366 · M.D. Anderson Cancer Center
CompletedPhase 1 / Phase 22015-07-084
Chlorhexidine and Essential Oil Mouthwashes on Human Beta-Defensin 2 (hbD2) and Kathelicidin (LL-37) Saliva Levels
NCT04946617 · Istanbul Medeniyet University
Status unknown2021-07-20120
Cathelicidin LL-37 Levels in the GCF and the Saliva of Smokers and Non-smokers With Stage III,IV Periodontitis
NCT04861493 · Cairo University
Completed2021-02-2360
Cathelicidin and Vitamin D: Impact on Populations At-Risk and With COPD
NCT02464059 · University of North Carolina, Chapel Hill
CompletedPhase 22015-11-1023
Salivary TAS, TOS, LL-37 and Dental Status in Passive Smoking Children
NCT04292548 · Merve Erkmen Almaz
Completed2016-11-16180
Efficacy of LL-37 Cream on Bacteria Colonization, Inflammation Response and Healing Rate of Diabetic Foot Ulcers
NCT04098562 · Fakultas Kedokteran Universitas Indonesia
Status unknownPhase 22019-1040
Effects of Smoking and Vitamin D3 on the Levels of Human Cathelicidin Peptide LL-37
NCT03923218 · Gazi University
Completed2011-1260
Passive Smoking and LL-37 in Children
NCT03639376 · Kırıkkale University
Completed2016-11180
Comparison of Cathelicidin Expression in Skin and Saliva in Patients With Atopic Dermatitis and Psoriasis
NCT00407979 · National Institute of Allergy and Infectious Diseases (NIAID)
Completed2005-0780
Effect of Pimecrolimus Cream on Cathelicidin Levels in Subjects With Eczema
NCT00946478 · University of California, San Diego
CompletedNot applicable2009-1040

VIP

StudyStatusPhaseStartPeople
Inhaled ZYESAMI (Aviptadil Acetate) for Treatment of Severe COVID-19
NCT05137795 · APR Applied Pharma Research s.a.
WithdrawnPhase 32021-12-150
I-SPY COVID-19 TRIAL: An Adaptive Platform Trial for Critically Ill Patients
NCT04488081 · QuantumLeap Healthcare Collaborative
Active, not recruitingPhase 22020-07-311500
ACTIV-3b: Therapeutics for Severely Ill Inpatients With COVID-19
NCT04843761 · National Institute of Allergy and Infectious Diseases (NIAID)
CompletedPhase 32021-04-20473
Aviptadil for Severely Ill Inpatients With COVID-19 (An ACTIV-3b/TESICO Treatment Trial)
NCT06729606 · National Institute of Allergy and Infectious Diseases (NIAID)
CompletedPhase 32021-04-20471
Inhaled Aviptadil for the Treatment of COVID-19 in Patients at High Risk for ARDS
NCT04536350 · Prof. Dr. Jörg Leuppi
TerminatedPhase 22021-05-1883
Intravenous Aviptadil for Critical COVID-19 With Respiratory Failure
NCT04311697 · APR Applied Pharma Research s.a.
CompletedPhase 2 / Phase 32020-05-15203
A Clinical Study Evaluating Inhaled Aviptadil on COVID-19
NCT04844580 · Centurion Pharma
CompletedPhase 22021-03-1080
Inhaled ZYESAMI™ (Aviptadil Acetate) for the Treatment of Severe COVID-19
NCT04360096 · APR Applied Pharma Research s.a.
TerminatedPhase 2 / Phase 32021-02-15144
ZYESAMI (Aviptadil) Intermediate Population Expanded Access Protocol (SAMICARE)
NCT04453839 · APR Applied Pharma Research s.a.
NO_LONGER_AVAILABLE
Phase I Study of Vasoactive Intestinal Peptide in Patients With Acute Respiratory Distress Syndrome and Sepsis
NCT00004494 · Stony Brook University
CompletedPhase 11998-0918
The Effects of a Long-lasting Infusion of Vasoactive Intestinal Peptide (VIP) in Episodic Migraine Patients
NCT04260035 · Danish Headache Center
CompletedNot applicable2020-05-1921
The Effects of a Long-lasting Infusion of Vasoactive Intestinal Peptide (VIP) on Headache, Cranial Hemodynamic and Autonomic Symptoms in Healthy Volunteers
NCT03989817 · Danish Headache Center
CompletedNot applicable2019-06-1412
Effect of PACAP38/VIP on Migraineurs Measured by Magnetic Resonance
NCT01471990 · Glostrup University Hospital, Copenhagen
CompletedNot applicable2011-0524
Vasoactive Intestinal Peptide in COPD
NCT00464932 · Medical University of Vienna
Completed2003-0634
Hemodynamic and Headache-Inducing Effect of Intravenous Vasoactive Intestinal Peptide in Migraineurs
NCT00272896 · Danish Headache Center
CompletedNot applicable2004-1012

Plecanatide

StudyStatusPhaseStartPeople
This is a Randomized, Double-blind, Placebo-controlled, Multicenter, Parallel-group Study of the Efficacy and Safety of 2 Weight-based Treatment Groups of Plecanatide Versus Placebo in Children and Adolescent Participants 6 to Less Than 18 Years of Age With FC
NCT07723924 · Bausch Health Americas, Inc.
RecruitingPhase 22026-08-18180
GCC Agonist Signal in the Small Intestine
NCT05107219 · University of Wisconsin, Madison
CompletedPhase 12022-11-3043
Efficacy and Safety of Plecanatide in Children 6 to <18 Years With Irritable Bowel Syndrome With Constipation (IBS-C)
NCT03596905 · Bausch Health Americas, Inc.
CompletedPhase 22018-06-30218
Efficacy and Safety of Plecanatide Comparing With Placebo in the Treatment of Functional Constipation
NCT05151328 · Shandong Luoxin Pharmaceutical Group Stock Co., Ltd.
CompletedPhase 32022-03-18648
Long Term Safety Study of Plecanatide
NCT02706483 · Bausch Health Americas, Inc.
CompletedPhase 32016-012272
12-Week Study of Plecanatide for CIC (The CIC3 Study)
NCT01982240 · Bausch Health Americas, Inc.
CompletedPhase 32013-111394
A Postmarketing Study of Plecanatide in Breast Milk of Lactating Women Treated With TRULANCE®
NCT03551873 · Bausch Health Americas, Inc.
Completed2018-06-217
An Efficacy and Safety Study of Plecanatide in Adolescents 12 to <18 Years of Age With Chronic Idiopathic Constipation
NCT03120520 · Bausch Health Americas, Inc.
CompletedPhase 22017-01124
Open-label Extension (OLE) Study of Plecanatide for Chronic Idiopathic Constipation (CIC)
NCT01919697 · Bausch Health Americas, Inc.
CompletedPhase 32013-082370
Second Plecanatide Study In Irritable Bowel Syndrome With Constipation (IBS-C)
NCT02493452 · Bausch Health Americas, Inc.
CompletedPhase 32015-061135
The Plecanatide Irritable Bowel Syndrome With Constipation Study (IBS-C)
NCT02387359 · Bausch Health Americas, Inc.
CompletedPhase 32014-121054
The Plecanatide Irritable Bowel Syndrome With Constipation Study (IBS-C)
NCT01722318 · Bausch Health Americas, Inc.
CompletedPhase 22012-11428
12-Week Study of Plecanatide for CIC (The National CIC3 Study)
NCT02122471 · Bausch Health Americas, Inc.
CompletedPhase 32014-041410
The Plecanatide Chronic Idiopathic Constipation (CIC) Study
NCT01429987 · Bausch Health Americas, Inc.
CompletedPhase 2 / Phase 32011-10951

Bremelanotide

StudyStatusPhaseStartPeople
Single Dose of Vyleesi in Lactating Female Subjects to Measure the Concentration of Bremelanotide in Breast Milk
NCT06867835 · Cosette Pharmaceuticals, Inc.
CompletedPhase 42025-07-1110
A Phase 2 Study Evaluating the Co-Administration of Bremelanotide With Tirzepatide for the Treatment of Obesity
NCT06565611 · Palatin Technologies, Inc
Active, not recruitingPhase 22024-08-05108
A Phase 3, Bridging, Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel-group Trial to Evaluate the Efficacy and Safety of Subcutaneously Administered Bremelanotide in Premenopausal Women With Hypoactive Sexual Desire Disorder (With or Without Decreased Arousal)
NCT04943068 · Kwang Dong Pharmaceutical co., ltd.
CompletedPhase 32021-05-10193
A Phase IIb, Multicenter, Open-Label, Prospective Study of Bremelanotide in Diabetic Kidney Disease
NCT05709444 · Palatin Technologies, Inc
CompletedPhase 22022-12-2616
Role of the Melanocortin-4 Receptor in Hypoactive Sexual Desire Disorder
NCT04179734 · Imperial College Healthcare NHS Trust
CompletedPhase 42019-10-0740
Study to Evaluate Rate of Nausea in Healthy Premenopausal Female Subjects Treated With Single Dose of Bremelanotide Alone or With Zofran
NCT03973047 · AMAG Pharmaceuticals, Inc.
CompletedPhase 12019-06-17228
1. Study to Evaluate the Efficacy/Safety of Bremelanotide in Premenopausal Women With Hypoactive Sexual Desire Disorder
NCT02333071 · Palatin Technologies, Inc
CompletedPhase 32014-12723
2. Study to Evaluate the Efficacy/Safety of Bremelanotide in Premenopausal Women With Hypoactive Sexual Desire Disorder
NCT02338960 · Palatin Technologies, Inc
CompletedPhase 32015-01714
Bremelanotide in Premenopausal Women With Female Sexual Arousal Disorder and/or Hypoactive Sexual Desire Disorder
NCT01382719 · Palatin Technologies, Inc
CompletedPhase 22011-06612
Evaluate the Safety and Efficacy of Bremelanotide in Women With Female Sexual Arousal Disorder (FSAD)
NCT00425256 · Palatin Technologies, Inc
CompletedPhase 22006-02

Neuropeptide Y

StudyStatusPhaseStartPeople
Sympathetic Transduction in Obesity-associated Hypertension (OB-HTN)
NCT04838678 · University of Texas Southwestern Medical Center
RecruitingEarly phase 12021-07-18100
Neuropeptide Y Regulates Neurogenic Pulp Inflammation
NCT06606236 · Institucion Universitaria Colegios de Colombia
CompletedNot applicable2024-02-0540
Moxonidine Effects on Neuropeptide Y
NCT05147753 · Aristotle University Of Thessaloniki
CompletedPhase 42010-01-1190
Sex Differences in Neuropeptide Y Serum, But Not in Fat Intake and Body Mass Index
NCT04650308 · Universitas Sumatera Utara
CompletedNot applicable2020-04-0262
Intranasal Neuropeptide Y in Clinical Trial in Level Two Trauma Patients for PTSD and Acute Stress Disorder
NCT04071600 · New York Medical College
Status unknownPhase 1 / Phase 22019-11-01117
Neuropeptide Y and Sympathovagal Balance
NCT03933787 · Eric Grouzmann
CompletedEarly phase 12018-06-057
Effect of DPP4 Inhibition on Vasoconstriction
NCT02639637 · Vanderbilt University
CompletedPhase 42015-1218
Intranasal Administration of Neuropeptide Y in Healthy Male Volunteers
NCT00748956 · Dennis Charney
CompletedPhase 22010-0110
A Dose Escalation Study of Intranasal Neuropeptide Y in Post Traumatic Stress Disorder (PTSD)
NCT01533519 · James Murrough
CompletedPhase 12012-1226
Neuropeptide Y (NPY) Regulation of Nociceptors
NCT00596193 · The University of Texas Health Science Center at San Antonio
Completed2001-0511

Thymopentin

StudyStatusPhaseStartPeople
The Prospective Clinical Study of Precision PRaG Therapy in Elderly Patients With Advanced Solid Malignant Tumors (PRaG9.0)
NCT06112041 · Second Affiliated Hospital of Soochow University
Not yet recruitingPhase 22023-10-2529
Study of Thymopentin in Patients After Curative Resection of Small Hepatocellular Carcinoma
NCT00460681 · Fudan University
Status unknownPhase 32007-02220
Double Blind Study of Thymopentin Effects on HIV-1 Infectivity of Blood Mononuclear Cells and Semen in HIV Infected Patients
NCT00002049 · Immunobiology Research Institute
CompletedNot applicable
The Effects of Thymopentin on HIV Infectivity of Blood Cells and Semen in HIV-Infected Patients
NCT00002289 · Immunobiology Research Institute
CompletedNot applicable
Double-Blind Study of Timunox (Thymopentin) in Asymptomatic HIV-Infected Patients Receiving Either Mono (AZT or ddI) or Combination (AZT / ddI or AZT / ddC) Anti-Retroviral Therapy
NCT00002109 · Immunobiology Research Institute
CompletedPhase 3
A Study of Thymopentin Effects on HIV-1 Infectivity of Blood Mononuclear Cells and Semen in HIV Infected Patients
NCT00002050 · Immunobiology Research Institute
CompletedNot applicable
Double Blind Study of Thymopentin Effects on Patients With HIV-1 Infection
NCT00002051 · Immunobiology Research Institute
CompletedNot applicable
Double Blind Study of Thymopentin Effects on Patients With HIV-1 Infection
NCT00002066 · Immunobiology Research Institute
CompletedNot applicable
A Study of Timunox (Thymopentin) in HIV-Infected Patients Receiving Other Anti-HIV Drugs
NCT00002332 · Immunobiology Research Institute
CompletedPhase 260

Nisotirostide

StudyStatusPhaseStartPeople
A Study of LY3457263 Compared With Placebo in Participants With Type 2 Diabetes on a Stable Dose of Semaglutide or Tirzepatide
NCT06897475 · Eli Lilly and Company
RecruitingPhase 22025-03-28200
A Study of LY3457263 Alone and in Combination With Dulaglutide (LY2189265) in Participants With Type 2 Diabetes
NCT05377333 · Eli Lilly and Company
CompletedPhase 12022-06-0294
A Study of LY3457263 in Obese Participants
NCT05582096 · Eli Lilly and Company
CompletedPhase 12022-11-1138
A Study of LY3457263 in Healthy Participants and Participants With Type 2 Diabetes
NCT04641312 · Eli Lilly and Company
CompletedPhase 12020-11-2567

Humanin

StudyStatusPhaseStartPeople
Comparison of the Effects of General Anesthesia and Combined Spinal-Epidural Anesthesia on Ferroptosis, Humanin and MOTS-c Levels in Renal Transplantation
NCT07678073 · University of Gaziantep
RecruitingNot applicable2026-03-0168
Clinical Value of Plasma Humanin in Acute Kidney Injury
NCT06105229 · Guangdong Provincial People's Hospital
Status unknown2022-08-0160
Humanin Isoforms in Cardiac Muscle and Blood Plasma and Major Complications After Cardiac Operation
NCT03431844 · University of Tartu
Completed2018-01-01106

Melanotan II

StudyStatusPhaseStartPeople
Melanotan II (MT-II) as an Adjunct to NB-UVB Phototherapy for Repigmentation in Stable Nonsegmental Vitiligo
NCT07437560 · Hudson Biotech
RecruitingPhase 22026-02-0260
Psychological Effects of Methylenedioxymethamphetamine (MDMA) When Administered to Healthy Volunteers (MT-2)
NCT04073433 · Resilient Pharmaceuticals
WithdrawnPhase 12024-120

TB-500

StudyStatusPhaseStartPeople
TB-500 (Thymosin Beta 4 17-23 Fragment) for Cardiovascular Biomarkers in Stable ASCVD
NCT07487363 · Hudson Biotech
RecruitingPhase 1 / Phase 22026-02-0580

Enfuvirtide

StudyStatusPhaseStartPeople
Intensification With Enfuvirtide in Naive HIV-infected Patients (ANRS130)
NCT00302822 · French National Agency for Research on AIDS and Viral Hepatitis
CompletedPhase 32006-04195
Early Intensification of Antiretroviral Therapy Including Enfuvirtide in HIV-1-Related Progressive Multifocal Leucoencephalopathy (ANRS125)
NCT00120367 · French National Agency for Research on AIDS and Viral Hepatitis
CompletedPhase 22005-0430
Optimized Antiretroviral Therapy During Allogeneic Hematopoietic Stem Cell Transplantation in HIV-1 Individuals
NCT01836068 · Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
CompletedEarly phase 12013-0611
Optimizing Treatment for Treatment-Experienced, HIV-Infected People
NCT00537394 · National Institute of Allergy and Infectious Diseases (NIAID)
CompletedPhase 32008-01517
Study of a New Anti-HIV Drug, T-20, in HIV-Infected Children
NCT00001118 · National Institute of Allergy and Infectious Diseases (NIAID)
CompletedPhase 124
Adding New Drugs for HIV Infected Patients Failing Current Therapy
NCT00031044 · National Institute of Allergy and Infectious Diseases (NIAID)
CompletedPhase 1 / Phase 250
Effect of an Enfuvirtide-based Anti-HIV Drug Regimen on Latent HIV Reservoirs in Treatment Naive Adults
NCT00051831 · National Institute of Allergy and Infectious Diseases (NIAID)
CompletedNot applicable2003-1019
A Study to Evaluate of the Efficacy of Enfuvirtide During the Induction Phase of Therapy
NCT00344760 · University of Maryland, Baltimore
CompletedPhase 42005-012
Evaluating the Effect of CHanging EnfuvirtidE to Raltegravir in HIV Infected Subjects
NCT00529243 · Kaiser Permanente
CompletedPhase 32007-0952
A 48 Week Study Comparing Treatment With Saquinavir + Lopinavir/Ritonavir in Combination With Enfuvirtide HAART Versus Saquinavir + Lopinavir/Ritonavir + Other Nucleoside Combinations to See the Efficacy of These Treatments in Patients Infected With HIV-1
NCT00100984 · Hoffmann-La Roche
TerminatedPhase 42004-07-218
A Study of Enfuvirtide (Fuzeon) in Patients With Advanced Human Immunodeficiency Virus-1 (HIV-1) Infection
NCT02569502 · Hoffmann-La Roche
CompletedPhase 42005-046
QUALITE Study - A Study of Fuzeon (Enfuvirtide) in Treatment-Experienced Patients With Human Immunodeficiency Virus-1 (HIV-1) Infection
NCT00232908 · Hoffmann-La Roche
CompletedPhase 42004-06361
A Study Comparing the Efficacy and Safety of Once-Daily Fuzeon (Enfuvirtide) Dosing Versus the Currently Recommended Twice-Daily Dosing in Human Immunodeficiency Virus-Type 1 (HIV-1) Infected Patients
NCT00089492 · Hoffmann-La Roche
CompletedPhase 22004-0764
An Observational Study of Induction Therapy With Fuzeon (Enfuvirtide) in Combination With Antiretroviral Drugs in Patients With HIV-1 Infection
NCT01902615 · Hoffmann-La Roche
Completed2001-0158
ESP Study: A Study to Assess the Effect of Adding Fuzeon (Enfuvirtide) to an Antiretroviral Regimen in Fuzeon-Naive Patients With Sustained HIV Viral Suppression.
NCT00461266 · Hoffmann-La Roche
WithdrawnPhase 42007-040

Peptide YY

StudyStatusPhaseStartPeople
L-Cell Activity in Small Intestine as Biliopancreatic Loop in Obese Patients With DM2 Submitted to RYGBP
NCT05446415 · University of Sao Paulo General Hospital
Status unknownNot applicable2020-02-0520
APPETITE: linguAl PYY3-36 on aPpEtite and acuTe Energy InTakE
NCT05110664 · University College, London
Status unknown2022-0240
Macronutrient Regulation of Ghrelin and Peptide YY
NCT02464514 · Duke University
CompletedNot applicable2004-0128
Role of the Gut Sweet Taste Receptor in the Secretion of Glucagon-like Peptide-1 and Peptide YY
NCT01304823 · University Hospital, Basel, Switzerland
CompletedPhase 12010-0610
Degradation of the Anorexic Hormone Peptide YY
NCT02493959 · Hvidovre University Hospital
CompletedEarly phase 12014-058
Effects of Intravenous Infusions of Gut Hormones on Appetite and Metabolism.
NCT00940134 · University of Copenhagen
CompletedNot applicable2011-0324
Sweet Taste Receptors and the Secretion of Glucagon-like Peptide-1 and Peptide YY
NCT01088841 · University Hospital, Basel, Switzerland
CompletedPhase 12009-0416
The Role of Peptide YY (PYY)Infusions in Inhibiting Food Intake.
NCT00259246 · University of Copenhagen
CompletedNot applicable2004-0624
The Role of Peptide YY (PYY)in Inhibiting Food Intake.
NCT00259233 · University of Copenhagen
CompletedNot applicable2005-0324
Oral Administration of Peptides; Absorption From Gastrointestinal Tract
NCT00468884 · University Hospital, Basel, Switzerland
CompletedPhase 12006-1012
A Study of Nasal PYY3-36 and Placebo for Weight Loss in Obese Subjects
NCT00537420 · Nastech Pharmaceutical Company, Inc.
CompletedPhase 22007-10551
Effects of Rosiglitazone on Serum Ghrelin and Peptide YY Levels
NCT00522470 · Baskent University
CompletedPhase 4
Safety, Toleration and Pharmacokinetics of Single Intravenous Doses of Peptide YY in Overweight Adults
NCT00331175 · Pfizer
CompletedPhase 12006-0731

Larazotide

StudyStatusPhaseStartPeople
AT1001 for the Treatment of Long COVID
NCT05747534 · Massachusetts General Hospital
CompletedPhase 22023-05-31107
AT1001 for the Treatment of COVID-19 Related MIS-C
NCT05022303 · Massachusetts General Hospital
TerminatedPhase 22021-10-0112
Study to Evaluate the Efficacy and Safety of Larazotide Acetate for the Relief of CeD Symptoms
NCT03569007 · 9 Meters Biopharma, Inc.
TerminatedPhase 32019-05-29307
Randomized, Double-Blind, Placebo-Controlled Study of Larazotide Acetate in Subjects With Active Celiac Disease
NCT00620451 · 9 Meters Biopharma, Inc.
CompletedPhase 22008-02105
Study of the Efficacy of Larazotide Acetate to Treat Celiac Disease
NCT00889473 · 9 Meters Biopharma, Inc.
CompletedPhase 22009-0442
A Double-blind Placebo-controlled Study to Evaluate Larazotide Acetate for the Treatment of Celiac Disease
NCT01396213 · 9 Meters Biopharma, Inc.
CompletedPhase 22011-11-07342
Study to Assess the Efficacy of Larazotide Acetate for the Treatment of Celiac Disease
NCT00492960 · 9 Meters Biopharma, Inc.
CompletedPhase 22007-08171
Safety of Larazotide Acetate in Healthy Volunteers
NCT00386490 · 9 Meters Biopharma, Inc.
CompletedPhase 12006-01-1024
Safety and Tolerability Study of Larazotide Acetate in Celiac Disease Subjects
NCT00362856 · 9 Meters Biopharma, Inc.
CompletedPhase 22006-09-1380
Safety Study of Larazotide Acetate to Treat Celiac Disease.
NCT00386165 · 9 Meters Biopharma, Inc.
CompletedPhase 12005-11-2921

TRH (thyrotropin-releasing hormone)

StudyStatusPhaseStartPeople
Study of Resistance to Thyroid Hormone After Long-term Exposure in People With Thyroid Cancer
NCT04868045 · Memorial Sloan Kettering Cancer Center
WithdrawnPhase 12021-04-270
Mechanistic Study of Subclinical Hypothyroidism In the Elderly
NCT02399475 · University of Pennsylvania
CompletedNot applicable2015-01-0114
Study of Thyrotropin-Releasing Hormone in Normal Volunteers and in Patients With Thyroid or Pituitary Abnormalities
NCT00054756 · National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
CompletedPhase 22003-02-0796
Evaluation of Synthetic Thyrotropin Releasing Hormone (TRH) as a Treatment for Cancer-related Fatigue
NCT00790296 · UConn Health
TerminatedPhase 22006-1211
Pharmacogenomic Response to Thyrotropin-Releasing Hormone Stimulation in Healthy Volunteers: The Influence of a Common Type 2 Deiodinase Genetic Polymorphism on Serum T3
NCT00812149 · National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Completed2008-12-1786
Study of Antenatal Thyrotropin-Releasing Hormone in Women in Premature Labor to Prevent Lung Disease in Preterm Infants
NCT00004840 · Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
CompletedNot applicable1998-05996
Phase III Randomized, Double-Blind, Placebo-Controlled Study of Antenatal Thyrotropin-Releasing Hormone in Pregnant Women With Threatened Premature Delivery
NCT00004778 · National Center for Research Resources (NCRR)
CompletedPhase 31993-081090

Orexin-A

StudyStatusPhaseStartPeople
Spectrometry (MRM) Versus I 125 Radioimmunoassay (RIA) for Quantification of Orexin-A of Patients With Hypersomnolence
NCT05615584 · University Hospital, Montpellier
CompletedNot applicable2023-02-15117
Digital Addiction, Sleep Quality and Orexin-A Level
NCT06738524 · Amasya University
CompletedNot applicable2024-02-0142
Orexin-A Levels in Insomnia Patients
NCT05664295 · Muğla Sıtkı Koçman University
Completed2022-12-3060
The Value of Combined Detection of Orexin-A, HLA Gene, PSG and MSLT in the Evaluation of Patients With Narcolepsy
NCT04940806 · Qianfoshan Hospital
Status unknown2021-05-01120
Plasma Orexin A and mRNA Expression Levels of Pre-pro-orexin Gene in Attention-Deficit Hyperactivity Disorder
NCT02074176 · National Taiwan University Hospital
Status unknown2011-0150
Difference of Plasma Orexin A Levels Between Elderly and Young Patients at Emergence
NCT01478906 · Xijing Hospital
Status unknown2011-0740

Efpeglenatide

Argireline

StudyStatusPhaseStartPeople
Topical Acetyl Hexapeptide-8 and the Cosmetic Appearance of Oily Skin
NCT02597777 · University of California, Davis
CompletedNot applicable2016-0114
Acetyl Hexapeptide-8 for Blepharospasm
NCT01750346 · National Institute of Neurological Disorders and Stroke (NINDS)
TerminatedPhase 22012-118
A Study of Acetyl Hexapeptide-8 (AH8) in Treatment of Blepharospasm
NCT00942851 · National Institute of Neurological Disorders and Stroke (NINDS)
CompletedPhase 1 / Phase 22009-0724
Argireline in Treatment of Periorbital Wrinkles
NCT01381484 · Mahidol University
CompletedPhase 32009-0370

Nesfatin-1

StudyStatusPhaseStartPeople
Serum Nesfatin-1 and Human Cartilage Glycoprotein-39 Levels in Knee Osteoarthritis
NCT06254976 · Kayseri City Hospital
CompletedNot applicable2022-06-0130
Nesfatin-1 Level in Patients With Type 2 Diabetes, Insulin Resistance and Obesity
NCT04298515 · Istanbul Medeniyet University
Status unknownNot applicable2020-03-02180
Role of Nesfatin-1 and Nicotinamide in Infertile Women With Polycystic Ovary Syndrome
NCT03870035 · Assiut University
Status unknown2019-05-0156
Cord Blood Nesfatin-1 and Irisin in the Intrauterine Growth Restricted Fetuses
NCT03808571 · Yuzuncu Yil University
Completed2018-01-0166

MK-677

StudyStatusPhaseStartPeople
The Impact of Ibutamoren on Nonalcoholic Fatty Liver Disease
NCT05364684 · Massachusetts General Hospital
CompletedPhase 22022-08-1012
Efficacy and Safety of an Oral Growth Hormone Drug in the Treatment of Fibromyalgia
NCT00116129 · Bennett, Robert, M.D.
CompletedPhase 22005-0764
Effects of an Oral GH Secretagogue (MK-677) on Body Composition and Functional Ability of Older Adults
NCT00474279 · University of Virginia
CompletedPhase 1 / Phase 21998-0772

ARA-290

StudyStatusPhaseStartPeople
Study of Efficacy of ARA 290 on Corneal Nerve Fiber Density and Neuropathic Symptoms of Subjects With Sarcoidosis
NCT02039687 · Araim Pharmaceuticals, Inc.
CompletedPhase 22014-0164
ARA290 in T2D (Effects of ARA 290, an Erythropoietin Analogue) in Prediabetes and Type 2 Diabetes)
NCT01933529 · Claes-Göran Östenson
Status unknownPhase 22013-1024

Ipamorelin

StudyStatusPhaseStartPeople
Safety and Efficacy of Ipamorelin for Management of Post-Operative Ileus
NCT00672074 · Helsinn Therapeutics (U.S.), Inc
CompletedPhase 22008-04117
Safety and Efficacy of Ipamorelin Compared to Placebo for the Recovery of Gastrointestinal Function
NCT01280344 · Helsinn Therapeutics (U.S.), Inc
CompletedPhase 22011-04320

CJC-1295

StudyStatusPhaseStartPeople
A Study to Evaluate CJC 1295 in HIV Patients With Visceral Obesity
NCT00267527 · ConjuChem
TerminatedPhase 22005-12120

Peptide bioregulators (Khavinson peptides)

StudyStatusPhaseStartPeople
Prospective Evaluation of Strontium in Patients After CardioGen-82 PET MPI Scanning
NCT01424774 · Bracco Diagnostics, Inc
Completed2011-09155

No registered human trials found

5-Amino-1MQ, Adipotide, AHK-Cu, AOD-9604, B7-33, Cortistatin, Dihexa, DSIP, Epitalon, Follistatin 344, FOXO4-DRI, GHK, GHRP-2, GHRP-6, Gonadorelin, Hexarelin, HGH Fragment 176-191, IGF-1 DES, IGF-1 LR3, KPV, Matrixyl, MGF, Modified GRF 1-29, N-Acetyl Selank, NA-Semax Amidate, P21, PE-22-28, PEG-MGF, Pinealon, PNC-27, PTD-DBM, Selank, Semax, Sermorelin, SLU-PP-332, SNAP-8, Thymalin, Thymulin

Searches use each profile's name and main aliases. A missing registration is not proof that no human study exists, but most published human research in the U.S. and Europe is registered.

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