Semaglutide: Participants will receive Semaglutide administered subcutaneously.
Tirzepatide: Participants will receive Tirzepatide administered subcutaneously.
Berobenatide: Participants will receive berobenatide solution for injection as subcutaneous injection.
The purpose of this study is to learn about the safety and effectiveness of berobenatide in adults with overweight or obesity who have already lost weight while taking semaglutide or tirzepatide. The study does not include people with diabetes.
Participants will be in the study for about 11 months.
| Facility | City | Region | Status |
|---|---|---|---|
| University of Alabama at Birmingham | Birmingham | Alabama | |
| Suncoast Clinical Research | New Port Richey | Florida | |
| Monroe Biomedical Research | Louisville | Kentucky | |
| Aa Mrc Llc | Flint | Michigan | |
| Clinical Research Professionals | Chesterfield | Missouri | |
| Mercury Street Medical Group, PLLC | Butte | Montana | |
| Accellacare - Wilmington | Wilmington | North Carolina | |
| Velocity Clinical Research, Mt. Auburn | Cincinnati | Ohio |
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07845500 on ClinicalTrials.gov ↗ ← All trials in the USA