LivingGLP1
Study S002280

A Parallel-group, Phase 1, Open-label Study to Investigate the Pharmacokinetics of LY3437943 in Participants With Renal Impairment Compared With Healthy Participants

Registration

Registration
NCT05611957
Study type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Phase
PHASE1
Masking
NONE
Status
COMPLETED
Enrollment
29
Start
2022-11-16
Primary completion
2023-09-05
Lead sponsor
Eli Lilly and Company
Conditions
Healthy; Renal Insufficiency
Interventions
DRUG:LY3437943
Results posted
FALSE
Individual participant data sharing
NO
Secondary identifiers
OTHER:J1I-MC-GZBL

Registered primary outcomes

  • Pharmacokinetics (PK): Area under the concentration versus time curve from time zero to infinity (AUC0-∞) of LY3437943 [Predose up to 31 days postdose]
  • PK: Maximum observed concentration (Cmax) of LY3437943 [Predose up to 31 days postdose]

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