LivingGLP1
Study S001636

A Multiple Dose Study in Healthy Overweight and Obese Participants to Investigate the Safety, Tolerability, and Pharmacokinetics of LY3502970

Registration

Registration
NCT05313802
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
DOUBLE
Status
COMPLETED
Enrollment
72
Start
2022-05-26
Primary completion
2022-09-09
Lead sponsor
Eli Lilly and Company
Conditions
Healthy; Obese
Interventions
DRUG:LY3502970
Results posted
TRUE
Individual participant data sharing
NO
Secondary identifiers
OTHER:J2A-MC-GZGK

Registered primary outcomes

  • Number of Participants With One or More Treatment Emergent Adverse Events (TEAEs) and Serious Adverse Event(s) (SAEs) Considered by the Investigator to be Related to Study Drug Administration [Baseline up to Day 42]

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