LivingGLP1
Study S003318

A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Multi-Center, Phase II Study to Evaluate the Efficacy, Safety, and Tolerability of Once-Daily RO7795081 Administered for 38 Weeks to Participants With Obesity or Overweight With at Least One Weight-Related Comorbidity

Registration

Registration
NCT07081958
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
DOUBLE
Status
COMPLETED
Enrollment
352
Start
2025-07-29
Primary completion
2026-04-28
Lead sponsor
Hoffmann-La Roche
Conditions
Obesity or Overweight
Interventions
DRUG:RO7795081; DRUG:Placebo
Results posted
FALSE
Individual participant data sharing
YES

Registered primary outcomes

  • Percent Change in Body Weight From Baseline to Week 30 [Baseline to Week 30]

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