drugset / Trial / NCT05445232

A Drug-Drug Interaction (DDI) Study of LY3437943 in Obese Participants

NCT05445232

Phase 1 Completed 32 enrolled Eli Lilly and Company
Non-randomizedSequentialOpen-labelBasic science

Summary

The main purpose of this study is to determine the effect of LY3437943 when administered subcutaneously on the levels of midazolam, warfarin and caffeine in the blood stream when administered orally as a drug cocktail in obese participants. This study will last up to approximately 25 weeks for each participant.

Timeline

Start
2022-07-08
Primary completion
2023-02-24
Completion
2023-02-24

Drugs

EvaluationDrugModalityDoseRoute
Subject Caffeine Small molecule Oral
Subject Midazolam Small molecule Oral
Subject Retatrutide Protein / enzyme biologic Subcutaneous
Subject Warfarin Small molecule Oral

Indications