drugset / Trial / NCT06039826

A Study of LY3437943 in Postmenopausal Female Participants Who Are Overweight or Obese

NCT06039826

Phase 1 Completed 46 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 combined oral contraceptive (COC) ethinyl estradiol and drospirenone in the blood stream in postmenopausal female participants who are overweight or obese. The safety and tolerability of LY3437943 when administered with COC will also be evaluated. This study will last up to approximately 29 weeks for each participant.

Timeline

Start
2023-09-12
Primary completion
2024-07-11
Completion
2024-07-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Retatrutide Protein / enzyme biologic Subcutaneous
Subject drospirenone Unknown Oral
Subject ethinyl estradiol Small molecule Oral

Indications