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A Study of Tirzepatide (LY3298176) in Healthy Lactating Females

Sponsored by Eli Lilly and Company

About this trial

Last updated 2 years ago

Study ID

18614

Status

Recruiting

Type

Interventional

Phase

Phase 1

Placebo

No

Accepting

18-75 Years
18+ Years
Female
Female

Trial Timing

Ended a year ago

What is this trial about?

The main purpose of this study is to look if the study drug, tirzepatide, gets into the breast milk and if yes, how long it takes the body to get rid of it. The study drug will be given as a single injection under the skin in healthy lactating females. For each participant, the total duration of the study will be approximately 8 weeks, including screening.

What are the participation requirements?

Yes

Inclusion Criteria

- Participants who are overtly healthy females as determined by medical evaluation

- Female participants who delivered normal-term infant (at least 37 weeks gestation) and are at least 6 weeks postpartum at the time of screening

- Body mass index (BMI) between 18.5 and 40.0 kilograms per meter squared (kg/m²), inclusive

- Female participants who has well-established lactation and is breastfeeding her infant. Note: Breastfeeding must be discontinued prior to the administration of tirzepatide on Day 1 and not resumed for the remaining duration of the study until a follow-up visit (or for total of 29 days after tirzepatide dosing for participants who discontinue early).

No

Exclusion Criteria

- Have a history of inadequate lactation (for multiparous females who have previously breastfed)

- Have confirmed type 1 or type 2 diabetes mellitus

- Regularly use known drugs of abuse or show positive findings on drug screen

Locations

Location

Status

Recruiting