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NCT04934696 · ClinicalTrials.gov registry record · Phase 1
A Study to Characterize the Drug Levels of an Oral Contraceptive With and Without BMS-986166 in Healthy Female Participants of Childbearing Potential
A Phase 1 study of Healthy Participants, sponsored by Bristol-Myers Squibb.
- Completed
- Registry status
- Phase 1
- Development phase
- 25
- Enrollment target
- 1
- Study location
NCT04934696 is a Phase 1 study of Healthy Participants that has completed, run by Bristol-Myers Squibb. The registered enrollment target is 25 participants, below the 65-participant average among 119 other Healthy Participants trials with a reported enrollment target (62% lower). The trial reports 1 study location across 1 state.
The verdict
NCT04934696, a Phase 1 study of Healthy Participants, has completed, sponsored by Bristol-Myers Squibb.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 25 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to investigate the potential for a drug-drug interaction (DDI) when BMS-986166 and hormonal oral contraceptives are co-administered.
Conditions Studied
Interventions
- DRUG BMS-986166
- DRUG Oral contraceptive
Study Locations (1)
California
- West Coast Clinical Trials Global - Cypress
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 25 participants |
| Start Date | 2021-08-03 |
| Est. Completion | 2022-01-25 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04934696
The ClinicalTrials.gov registry entry for NCT04934696 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 25 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 65-participant average among 119 other Healthy Participants trials with a reported enrollment target (62% lower). The listed sponsor is Bristol-Myers Squibb, which has 1,025 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Healthy Participants appearing as the primary indexed condition, and to 2 interventions - of which BMS-986166 is the first listed.
NCT04934696 reports 1 study location spanning 1 distinct geographic area - top geographies include California.
Frequently Asked Questions
What is clinical trial NCT04934696 about?
NCT04934696 is a clinical study titled "A Study to Characterize the Drug Levels of an Oral Contraceptive With and Without BMS-986166 in Healthy Female Participants of Childbearing Potential". The purpose of this study is to investigate the potential for a drug-drug interaction (DDI) when BMS-986166 and hormonal oral contraceptives are co-administered.
What is the current status of trial NCT04934696?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 25 participants. The study started on 2021-08-03. Estimated completion is 2022-01-25.
What conditions does trial NCT04934696 study?
This clinical trial studies the following conditions: Healthy Participants.
What interventions are being tested in trial NCT04934696?
The interventions under investigation include: BMS-986166 (DRUG), Oral contraceptive (DRUG).
Who is sponsoring clinical trial NCT04934696?
This trial is sponsored by Bristol-Myers Squibb, which has 1,025 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT04934696 being conducted?
This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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