LivingGLP1
Study S002374

A Master Protocol to Investigate the Efficacy and Safety of Orforglipron Tablet Once Daily Compared With Placebo in Participants With Obesity or Overweight With and Without Type 2 Diabetes

Registration

Registration
NCT06993792
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
DOUBLE
Status
ACTIVE_NOT_RECRUITING
Enrollment
1400
Start
2025-05-15
Primary completion
2027-08
Lead sponsor
Eli Lilly and Company
Conditions
Obesity; Overweight; Type 2 Diabetes
Interventions
DRUG:Orforglipron; DRUG:Placebo
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
CTIS:2025-521098-14-00; OTHER:J2A-MC-GZPO; OTHER:J2A-MC-GZP1; OTHER:J2A-MC-GZP2; NIH:2025

Registered primary outcomes

  • Number of Participants Allocated to Each Study [Baseline to Week 4]

Linked records (0)

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