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Taking peoplePhase 3

Tests petrelintide against placebo for weight management in adults with obesity

Tests petrelintide, a once-weekly drug, in adults with overweight or obesity.

Plain-language title generated from the registry record
Registry title: A Phase III Study to Evaluate the Efficacy and Safety of Petrelintide in Participants With Overweight or Obesity

Key facts

Where
Florence, Milan, Palermo, and Pisa, ItalySee the 5 sites
Phase
Phase 3

Where in Italy

  • Azienda Ospedaliero-Universitaria CareggiFlorence, ItalyNot yet recruiting
  • Centro Cardiologico Monzino S.p.A.Milan, ItalyNot yet recruiting
  • Ospedale San Raffaele S.r.l.Milan, ItalyNot yet recruiting
  • Azienda Ospedaliera Universitaria Policlinico Paolo GiacconePalermo, ItalyNot yet recruiting
  • Azienda Ospedaliero Universitaria PisanaPisa, ItalyNot yet recruiting

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
Hoffmann-La Roche
Trial code
NCT07843498EU 2026-526188-39-00
Record updated
5 November 2026
Original description
This study will evaluate the efficacy and safety of petrelintide compared with placebo, in conjunction with a reduced-calorie diet and increased physical activity, for weight management in participants living with overweight or obesity, at least one weight-related comorbidity, and without Type 2 Diabetes (T2D).Read full original descriptionShow less

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

This study will evaluate the efficacy and safety of petrelintide compared with placebo, in conjunction with a reduced-calorie diet and increased physical activity, for weight management in participants living with overweight or obesity, at least one weight-related comorbidity, and without Type 2 Diabetes (T2D).

Inclusion: Participants with BMI ≥ 30 kg/m² or BMI ≥ 27 kg/m² with at least one weight-related comorbidity; History of at least one self-reported unsuccessful dietary effort to lose body weight.

Exclusion: Current or previous treatment with petrelintide or any other amylin analog; Known history of Type 1 or Type 2 diabetes mellitus; HbA1c ≥ 48 mmol/mol (6.5%), measured by the central laboratory at screening.

ClinicalTrials.gov NCT07843498 · EU CTIS 2026-526188-39-00