A Study to Investigate the Interaction of BMS-986322 and a Combined Oral Hormonal Contraceptive (Ethinyl Estradiol [EE]/Norethindrone [NET]) in Healthy Female Participants

Completed · Phase 1

Conditions studied: Healthy Participants

In brief

The purpose of this study is to evaluate the effect of multiple doses of BMS-986322 on the pharmacokinetics (PK) of Loestrin components in healthy female participants.

Key facts

Study ID
NCT05579574
Run by
Bristol-Myers Squibb
People needed
42
Starts
2022-10-21
Expected to finish
2023-06-01
Last updated by the study team
2023-08-18

Who can join

Age: 18 and older, up to 40. Sex: female. Healthy volunteers: accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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