LivingGLP1
Study S001710

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
NCT06972459
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
DOUBLE
Status
ACTIVE_NOT_RECRUITING
Enrollment
800
Start
2025-05-15
Primary completion
2027-08
Lead sponsor
Eli Lilly and Company
Conditions
Obesity; Overweight
Interventions
DRUG:Orforglipron; DRUG:Placebo
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
CTIS:2025-521098-14-00; OTHER:J2A-MC-GZP1; OTHER:J2A-MC-GZPO; NIH:2025

Registered primary outcomes

  • Percent Change from Baseline in Body Weight [Baseline, Week 72]

Linked records (0)

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