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Retatrutide

LY3437943, LY-3437943

Quick Stats
Studies 83
Trials 32
Completed PHASE1 INTERVENTIONAL NCT06039826

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

View on ClinicalTrials.gov Updated Dec 15, 2025

Brief 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.

Interventions

Name: LY3437943
Type: DRUG
Description: Administered SC.
Name: Ethinyl Estradiol
Type: DRUG
Description: Administered orally
Name: Drospirenone
Type: DRUG
Description: Administered orally

Primary Outcomes

Measure: Pharmacokinetics (PK): Area Under the Concentration Versus Time Curve from Time zero to 24 Hours Postdose (AUC0-24) of Ethinyl Estradiol
TimeFrame: Predose on Day 1 up to 144 days postdose
Description: PK: AUC0-24 of Ethinyl Estradiol
Measure: PK: Maximum Observed Concentration (Cmax) of Ethinyl Estradiol
TimeFrame: Predose on Day 1 up to 144 days postdose
Description: PK: Cmax of Ethinyl Estradiol
Measure: PK: Time of Maximum Observed Concentration (Tmax) of Ethinyl Estradiol
TimeFrame: Predose on Day 1 up to 144 days postdose
Description: PK: Tmax of Ethinyl Estradiol
Measure: PK: Area Under the Concentration Versus Time Curve from Time zero to 24 Hours Postdose (AUC0-24) of Drospirenone
TimeFrame: Predose on Day 1 up to 144 days postdose
Description: PK: AUC0-24 of Drospirenone
Measure: PK: Maximum Observed Concentration (Cmax) of Drospirenone
TimeFrame: Predose on Day 1 up to 144 days postdose
Description: PK: Cmax of Drospirenone
Measure: PK: Time of Maximum Observed Concentration (Tmax) of Drospirenone
TimeFrame: Predose on Day 1 up to 144 days postdose
Description: PK: Tmax of Drospirenone

Trial Information

NCT ID

NCT06039826

Status

Completed

Study Type

INTERVENTIONAL

Phases

PHASE1

Sponsor

Eli Lilly and Company

Last Updated

December 15, 2025