DRUG
Ribupatide
SC Injection
Status
Active, not recruiting
Phase
Phase 2
Enrollment
264
Locations
35
Results
Not posted
Publications
0
Study summary
The primary objective of this study is to determine the effects of ribupatide administered by subcutaneous (SC) injection once weekly compared to placebo on percent change in body weight.
Interventions
DRUG
SC Injection
DRUG
SC Injection
Timeline
First posted
Mar 9, 2026
Study start
Mar 4, 2026
Primary completion
May 2027
Study completion
Jun 2027
Results posted
Not reported
Registry updated
Jul 15, 2026
Outcomes
Percent Change From Baseline in Body Weight at Week 48
Time frame · Baseline, Week 48
Percent of Participants with ≥5%, ≥10%, ≥15%, ≥20% and ≥25% Reduction From Baseline in Body Weight
Time frame · Baseline, Week 48
Change From Baseline in Waist Circumference
Time frame · Baseline, Week 48
Change From Baseline in Absolute Body Weight
Time frame · Baseline, Week 48
Change From Baseline in Body Mass Index (BMI)
Time frame · Baseline, Week 48
Percent Change From Baseline in Fasting Triglycerides
Time frame · Baseline, Week 48
Percent Change From Baseline in Fasting High-density Lipoprotein (HDL)-cholesterol
Time frame · Baseline, Week 48
Percent Change From Baseline in Fasting Non-HDL-cholesterol
Time frame · Baseline, Week 48
Percent Change From Baseline in Fasting Total Cholesterol
Time frame · Baseline, Week 48
Percent Change From Baseline in Fasting Low-density Lipoprotein (LDL)-cholesterol
Time frame · Baseline, Week 48
Percent Change From Baseline in Fasting Very Low-density Lipoprotein (VLDL)-cholesterol
Time frame · Baseline, Week 48
Eligibility
Key Inclusion Criteria: * BMI ≥35 kilograms per meter squared (kg/m\^2). * History of at least 1 self-reported unsuccessful effort to lose weight with diet and exercise within the prior 6 months. Key Exclusion Criteria: * Current diagnosis or history of diabetes mellitus, including type 1 diabetes mellitus (T1DM) or type 2 diabetes mellitus (T2DM), history of diabetic ketoacidosis, or hyperosmolar state/coma. * Started medications within 3 months prior to Screening that may cause significant weight gain, including, but not limited to, tricyclic antidepressants, atypical antipsychotics, and mood stabilizers. * Unstable weight defined as self-reported change in body weight exceeding 5% within 3 months prior to Screening. * Family or personal history of multiple endocrine neoplasia Type 2 or medullary thyroid cancer. * Uncontrolled hypertension or unstable cardiovascular disease. * History of chronic or acute pancreatitis. * Known clinically significant gastric-emptying abnormality or chronic treatment with medications that directly affect gastrointestinal motility. * History of suicide attempt. * History of significant active or unstable Major Depressive Disorder (MDD) or other severe psychiatric disorder within 2 years prior to Screening. * Received treatment with semaglutide, tirzepatide, glucagon-like peptide-1 receptor (GLP-1R) agonist, GLP-1R/glucose-dependent insulinotropic polypeptide receptor (GIPR), or glucagon receptor agonist within 3 months prior to Screening. Note: Additional inclusion/exclusion criteria may apply, per protocol.
Study locations
United States. Showing up to 24 locations stored in the fast local snapshot.
Kailera Clinical Site
Mesa, Arizona, United States
Kailera Clinical Site
Sun City West, Arizona, United States
Kailera Clinical Site
Irvine, California, United States
Kailera Clinical Site
Lake Forest, California, United States
Kailera Clinical Site
Lomita, California, United States
Kailera Clinical Site
Long Beach, California, United States
Kailera Clinical Site
Montclair, California, United States
Kailera Clinical Site
Rolling Hills Estates, California, United States
Kailera Clinical Site
San Diego, California, United States
Kailera Clinical Site
Santa Ana, California, United States
Kailera Clinical Site
Van Nuys, California, United States
Kailera Clinical Site
DeLand, Florida, United States
Kailera Clinical Site
Orlando, Florida, United States
Kailera Clinical Site
Orlando, Florida, United States
Kailera Clinical Site
The Villages, Florida, United States
Kailera Clinical Site
Decatur, Georgia, United States
Kailera Clinical Site
Woodstock, Georgia, United States
Kailera Clinical Site
Morton, Illinois, United States
Kailera Clinical Site
Indianapolis, Indiana, United States
Kailera Clinical Site
Louisville, Kentucky, United States
Kailera Clinical Site
Rockville, Maryland, United States
Kailera Clinical Site
St Louis, Missouri, United States
Kailera Clinical Site
Lincoln, Nebraska, United States
Kailera Clinical Site
Omaha, Nebraska, United States
Publications
No PMID-linked publications were present in this registry snapshot.
Related trials
The Cleveland Clinic · Metabolic Dysfunction-associated Steatotic Liver Disease (MASLD) · Non-Alcoholic Fatty Liver Disease
Phase 4
Recruiting
120
2026-07
Shahid Beheshti University of Medical Sciences · Heart Failure and Reduced Ejection Fraction · Obesity & Overweight
Phase 3
Not yet recruiting
60
2026-07
Alaa Sada · Mild Autonomous Cortisol Secretion (MACS) · Adrenalectomy; Status
Phase 2
Recruiting
34
2026-07
China-Japan Friendship Hospital · Obesity
Not applicable
Recruiting
400
2026-07
yifang zhu · Acute Ischemic Stroke (AIS)
Phase 2 / Phase 3
Not yet recruiting
430
2026-07
Johns Hopkins University · Central Centrifugal Cicatricial Alopecia (CCCA)
Phase 2
Not yet recruiting
20
2026-07
Milton S. Hershey Medical Center · Opioid Use Disorder · Opioid Abuse and Addiction
Phase 2
Recruiting
200
2026-07
Duke University · Idiopathic Intracranial Hypertension (IIH)
Phase 4
Not yet recruiting
60
2026-07
Related PeptideStat pages
Research pages describe evidence. Vendor pages, where available, describe independently tracked research-product listings and are not clinical recommendations.