LivingGLP1
Study S002183

Effect of Injection Site on the Relative Bioavailability of a Single Dose of LY3437943 in Healthy Participants With a High Body Mass Index

Registration

Registration
NCT05959096
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
NONE
Status
COMPLETED
Enrollment
85
Start
2023-07-18
Primary completion
2024-07-25
Lead sponsor
Eli Lilly and Company
Conditions
Healthy
Interventions
DRUG:LY3437943
Results posted
FALSE
Individual participant data sharing
NO
Secondary identifiers
OTHER:J1I-MC-GZBS

Registered primary outcomes

  • Part A: Pharmacokinetics (PK): Area Under the Plasma Concentration Versus Time Curve From Zero to Infinity (AUC[0-∞]) of LY3437943 [Predose on Day 1 up to 43 days postdose (Part A)]
  • Part A: PK: Maximum Concentration (Cmax) of LY3437943 [Predose on Day 1 up to 43 days postdose (Part A)]

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