LivingGLP1
Study S002053

A Multiple Dose Escalation Study in Chinese Participants With Overweight BMI or Obesity to Investigate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of LY3437943

Registration

Registration
NCT05548231
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
DOUBLE
Status
COMPLETED
Enrollment
32
Start
2022-10-24
Primary completion
2023-07-27
Lead sponsor
Eli Lilly and Company
Conditions
Overweight; Obesity
Interventions
DRUG:LY3437943; DRUG:Placebo
Results posted
FALSE
Individual participant data sharing
NO
Secondary identifiers
OTHER:J1I-MC-GZBE

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 through Week 20]

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