Petrelintide for weight loss in people with overweight/obesity and heart disease
Official title: A Phase III, Randomized, Double-Blind, Placebo Controlled, Parallel Group Study to Evaluate the Efficacy and Safety of Once Weekly Petrelintide Vs. Placebo in Participants With Overweight Or Obesity And Established Cardiovascular Disease
Run by Hoffmann-La Roche · NCT07843472 · Data updated 2026-11-12
This study tests whether petrelintide helps people with overweight or obesity and cardiovascular disease lose weight when added to a reduced-calorie diet and more physical activity, compared with a placebo.
Quick facts
| Phase | Phase 3 |
|---|---|
| Study type | Interventional |
| Ages | 40 Years and up |
| Sex | All |
| Enrollment | 2500 (estimated) |
| Sponsor | Hoffmann-La Roche Industry-sponsored |
| Locations | 3 sites (Anniston, Alabama and 2 other locations) |
| Status | Recruiting |
| Started | September 30, 2026 |
| Main results expected | July 28, 2030 |
| Study ends | October 6, 2030 |
| Registry record updated | October 7, 2026 |
| Trial ID | NCT07843472 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults with BMI ≥ 27 kg/m² and established cardiovascular disease who have tried but not succeeded with dieting before.
✕Probably not a fit
Individuals without overweight/obesity or with non-established cardiovascular disease, or those who cannot participate in the diet/exercise program, may not benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This Phase 3 interventional trial compares petrelintide to placebo in adults with BMI 27 or higher and established cardiovascular disease. All participants receive a structured lifestyle program that includes a reduced-calorie diet and increased physical activity. The study aims to determine the drug’s effect on weight change and safety over time. Excluded are individuals with type 1 diabetes or prior petrelintide or amylin analog use, and those who have not previously failed diet attempts. The trial is sponsored by Hoffmann-La Roche with Zealand Pharma and is conducted at multiple sites in the United States.
Why it matters
Potential benefit: If successful, participants could lose more weight and improve health markers related to obesity and cardiovascular disease.
How similar studies have gone: Prior studies of amylin analogs in weight management have shown potential benefits, though results vary by population and context.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Participants with BMI ≥ 27 kg/m² and established CVD * History of at least one self-reported unsuccessful dietary effort to lose body weight Exclusion Criteria: * Known history of Type 1 diabetes mellitus * Current or previous treatment with petrelintide or any other amylin analog
Where it's running
-
Pinnacle Research Group
Anniston, Alabama, United States Recruiting -
Institute for Metabolic Research Los Angeles
Los Angeles, California, United States Recruiting -
Progressive Medical Research
Port Orange, Florida, United States Recruiting
Study contacts
- Study coordinator: Reference Study ID Number: CC46446 https://forpatients.roche.com/No attachments to email below.
- Email: global-roche-genentech-trials@gene.com
- Phone: 888-662-6728 (U.S. and Canada)
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.