LivingGLP1
Study S003352

A Randomized, Double-Blind, Single-Ascending Dose and Multiple-Dose, Placebo-Controlled Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of LY3549492 in Healthy Subjects

Registration

Registration
NCT04758234
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
DOUBLE
Status
COMPLETED
Enrollment
54
Start
2021-02-22
Primary completion
2022-01-10
Lead sponsor
Eli Lilly and Company
Conditions
Healthy
Interventions
DRUG:LY3549492; DRUG:Placebo
Results posted
FALSE
Individual participant data sharing
NO
Secondary identifiers
OTHER:J3H-MC-GZNA

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 final follow-up at approximately Day 76]

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