A Phase III Study to Evaluate the Efficacy and Safety of Petrelintide in Participants With Overweight or Obesity

Part of paid clinical trials in Anniston, Alabama.

Sponsor
Hoffmann-La Roche
Study ID
NCT07843498
Phase
PHASE3
Status
Recruiting

Conditions

  • Obesity or Overweight

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Petrelintide — COMBINATION_PRODUCT
    Petrelintide will be administered subcutaneously (SC) using a drug-device combination product.
  • Placebo — COMBINATION_PRODUCT
    Petrelintide-matching placebo will be administered SC using a drug-device combination product.

Study Details

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).

Key Dates

First listed
Sep 28, 2026
Start date
Sep 30, 2026
Status verified
Oct 2026
Primary completion
Dec 21, 2028
Completion
Mar 22, 2029

Study Design

Enrollment
3,900 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: Petrelintide
  • Placebo Comparator: Placebo

Primary Outcome Measure

Percentage Change in Body Weight from Baseline [ Time Frame: From Baseline to Week 64 ]

Central Contacts

  • Reference Study ID Number: CC46368 https://forpatients.roche.com/No attachments to email below.
    888-662-6728 (U.S. and Canada)
  • Fastest Response: use the inquiry form. https://www.gene.com/contact-us/submit-medical-inquiry

Locations (3)

FacilityCityStateZIPSite coordinators
Pinnacle Research GroupAnnistonAlabama36207-
Progressive Medical ResearchPort OrangeFlorida32127-
Clinical Research AssociatesNashvilleTennessee37203-

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