LivingGLP1
Study S003326

A Phase 2, Parallel-Group, Double-Blind Study to Investigate Weight Management With LY3549492 Once Daily Compared With Placebo in Adult Participants With Obesity or Overweight

Registration

Registration
NCT06683508
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
DOUBLE
Status
COMPLETED
Enrollment
288
Start
2024-11-13
Primary completion
2026-01-07
Lead sponsor
Eli Lilly and Company
Conditions
Obesity; Overweight
Interventions
DRUG:LY3549492; DRUG:Placebo
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
OTHER:W8M-MC-GN01; OTHER:W8M-MC-CWMM

Registered primary outcomes

  • Percent Change from Baseline in Body Weight [Baseline, Week 36]

Linked records (0)

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