LivingGLP1
Study S000639

A Randomized, Double-Blind, Placebo- and Open-Label Active Comparator- Controlled, Parallel-Group, Multi-Center Phase II Study to Evaluate the Efficacy, Safety, and Tolerability of Once-Daily RO7795081 Administered for 30 Weeks to Participants With Type 2 Diabetes Mellitus

Registration

Registration
NCT07112872
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
DOUBLE
Status
ACTIVE_NOT_RECRUITING
Enrollment
330
Start
2025-08-19
Primary completion
2028-02-05
Lead sponsor
Hoffmann-La Roche
Conditions
Type 2 Diabetes Mellitus
Interventions
DRUG:RO7795081; DRUG:Semaglutide; DRUG:Placebo
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
CTIS:2024-520322-11-00

Registered primary outcomes

  • RO7795081 vs. Placebo: Change in Glycated Hemoglobin (HbA1c) from Baseline at Week 30 [Baseline to Week 30]

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