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NCT04016753 · ClinicalTrials.gov registry record · Phase 1
A Study Measuring the Effectiveness of BMS-986256 Combined With Oral Contraceptive in Healthy Female Participants
A Phase 1 study, sponsored by Bristol-Myers Squibb.
- Completed
- Registry status
- Phase 1
- Development phase
- 32
- Enrollment target
NCT04016753 is a Phase 1 study that has completed, run by Bristol-Myers Squibb. The registered enrollment target is 32 participants.
The verdict
NCT04016753, a Phase 1 study, has completed, sponsored by Bristol-Myers Squibb.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 32 participants
- Enrollment target
Study Summary
A comparative study of BMS-986256 with a combined oral contraceptive in healthy female participants to determine the effectiveness when taken together
Interventions
- DRUG Loestrin
- DRUG BMS-986256
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 32 participants |
| Start Date | 2019-08-05 |
| Est. Completion | 2020-02-21 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04016753
The ClinicalTrials.gov registry entry for NCT04016753 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 32 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.
NCT04016753 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT04016753 about?
NCT04016753 is a clinical study titled "A Study Measuring the Effectiveness of BMS-986256 Combined With Oral Contraceptive in Healthy Female Participants". A comparative study of BMS-986256 with a combined oral contraceptive in healthy female participants to determine the effectiveness when taken together
What is the current status of trial NCT04016753?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 32 participants. The study started on 2019-08-05. Estimated completion is 2020-02-21.
What interventions are being tested in trial NCT04016753?
The interventions under investigation include: Loestrin (DRUG), BMS-986256 (DRUG).
Who is sponsoring clinical trial NCT04016753?
This trial is sponsored by Bristol-Myers Squibb, which has 1,025 total clinical trials registered on ClinicalTrials.gov.
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