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Tirzepatide

Mounjaro, Zepbound, LY3298176

Quick Stats
Studies 183
Trials 100
Active Not Recruiting PHASE2 INTERVENTIONAL NCT06965413

A Study to Assess Efficacy, Safety, Tolerability, Pharmacokinetics (PK) and Pharmacodynamics (PD) of RO7204239 in Combination With Tirzepatide in Participants With Obesity or Overweight With At Least One Weight-related Comorbidity

View on ClinicalTrials.gov Updated Dec 15, 2025

Brief Summary

The main aim of the study is to assess the effect of RO7204239 in combination with tirzepatide, compared to placebo in combination with tirzepatide, on body weight loss after 48 weeks of treatment in adults with obesity or overweight with at least one weight-related comorbidity, but without diabetes mellitus (DM). The study comprises of a 4-week screening period; a 48-week core treatment period, where all participants will receive tirzepatide as background treatment and will be randomized to one of the 4 treatment arms; a 24-week treatment extension period, where participants will stop treatment with tirzepatide and a 24-week post-treatment follow-up (FU) period.

Interventions

Name: RO7204239
Type: DRUG
Description: RO7204239 or matching placebo will be administered as per the schedule specified in the arms.
Name: RO7204239 Matching Placebo
Type: DRUG
Description: RO7204239 matching placebo will be administered as per the schedule specified in the arm.
Name: Tirzepatide
Type: DRUG
Description: Tirzepatide will be administered as per the schedule specified in the arms.

Primary Outcomes

Measure: Percent Change From Baseline in Body Weight
TimeFrame: Baseline, Week 48
Description:

Trial Information

NCT ID

NCT06965413

Status

Active Not Recruiting

Study Type

INTERVENTIONAL

Phases

PHASE2

Sponsor

Hoffmann-La Roche

Last Updated

December 15, 2025