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NCT05891262 · ClinicalTrials.gov registry record · Phase 1
A Study to Evaluate the Drug-drug Interaction of BMS-986196 With Oral Contraceptives in Healthy Female Participants
A Phase 1 study, sponsored by Bristol-Myers Squibb.
- Completed
- Registry status
- Phase 1
- Development phase
- 15
- Enrollment target
NCT05891262 is a Phase 1 study that has completed, run by Bristol-Myers Squibb. The registered enrollment target is 15 participants.
The verdict
NCT05891262, a Phase 1 study, has completed, sponsored by Bristol-Myers Squibb.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 15 participants
- Enrollment target
Study Summary
The purpose of this study is to evaluate the effect of BMS-986196 when coadministered with combined hormonal oral contraceptives (ethinyl estradiol \[EE\] and norethindrone \[NET\]) in healthy female participants.
Interventions
- DRUG Loestrin
- DRUG BMS-986196
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 15 participants |
| Start Date | 2023-06-06 |
| Est. Completion | 2023-08-25 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05891262
The ClinicalTrials.gov registry entry for NCT05891262 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 15 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 Loestrin is the first listed.
NCT05891262 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT05891262 about?
NCT05891262 is a clinical study titled "A Study to Evaluate the Drug-drug Interaction of BMS-986196 With Oral Contraceptives in Healthy Female Participants". The purpose of this study is to evaluate the effect of BMS-986196 when coadministered with combined hormonal oral contraceptives (ethinyl estradiol \[EE\] and norethindrone \[NET\]) in healthy female participants.
What is the current status of trial NCT05891262?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 15 participants. The study started on 2023-06-06. Estimated completion is 2023-08-25.
What interventions are being tested in trial NCT05891262?
The interventions under investigation include: Loestrin (DRUG), BMS-986196 (DRUG).
Who is sponsoring clinical trial NCT05891262?
This trial is sponsored by Bristol-Myers Squibb, which has 1,025 total clinical trials registered on ClinicalTrials.gov.
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