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NCT05579574 · ClinicalTrials.gov registry record · Phase 1
A Study to Investigate the Interaction of BMS-986322 and a Combined Oral Hormonal Contraceptive (Ethinyl Estradiol [EE]/Norethindrone [NET]) in Healthy Female Participants
A Phase 1 study, sponsored by Bristol-Myers Squibb.
- Completed
- Registry status
- Phase 1
- Development phase
- 42
- Enrollment target
NCT05579574 is a Phase 1 study that has completed, run by Bristol-Myers Squibb. The registered enrollment target is 42 participants.
The verdict
NCT05579574, a Phase 1 study, has completed, sponsored by Bristol-Myers Squibb.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 42 participants
- Enrollment target
Study Summary
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.
Interventions
- DRUG BMS-986322
- DRUG Loestrin
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 42 participants |
| Start Date | 2022-10-21 |
| Est. Completion | 2023-06-01 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05579574
The ClinicalTrials.gov registry entry for NCT05579574 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 42 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Bristol-Myers Squibb, which has 1,025 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which BMS-986322 is the first listed.
NCT05579574 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT05579574 about?
NCT05579574 is a clinical study titled "A Study to Investigate the Interaction of BMS-986322 and a Combined Oral Hormonal Contraceptive (Ethinyl Estradiol [EE]/Norethindrone [NET]) in Healthy Female Participants". 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.
What is the current status of trial NCT05579574?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 42 participants. The study started on 2022-10-21. Estimated completion is 2023-06-01.
What interventions are being tested in trial NCT05579574?
The interventions under investigation include: BMS-986322 (DRUG), Loestrin (DRUG).
Who is sponsoring clinical trial NCT05579574?
This trial is sponsored by Bristol-Myers Squibb, which has 1,025 total clinical trials registered on ClinicalTrials.gov.
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