LivingGLP1
Study S003306

A Phase-1, Parallel-Design, Open-Label, Randomized, Multiple-Dose Escalation Study to Investigate the Safety, Tolerability, and Pharmacokinetics of LY3549492 in Healthy Participants With Overweight or Obesity

Registration

Registration
NCT07232732
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
NONE
Status
COMPLETED
Enrollment
120
Start
2025-10-27
Primary completion
2026-07-16
Lead sponsor
Eli Lilly and Company
Conditions
Healthy; Obesity; Overweight
Interventions
DRUG:LY3549492
Results posted
FALSE
Individual participant data sharing
NO
Secondary identifiers
OTHER:J3H-MC-GZNJ

Registered primary outcomes

  • Number of Participants with One or More Serious Adverse Event(s) (SAEs) Considered by the Investigator to be Related to Study Drug Administration [Baseline through end of the Follow-up Period (Week 10)]

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