LivingGLP1
Study S000218

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
NCT06972472
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
DOUBLE
Status
ACTIVE_NOT_RECRUITING
Enrollment
600
Start
2025-05-19
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-GZP2; OTHER:J2A-MC-GZPO; NIH:2025

Registered primary outcomes

  • Change from Baseline in Hemoglobin A1c (HbA1c) [Baseline, Week 40]

Linked records (0)

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