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NCT03262740 · ClinicalTrials.gov registry record · Phase 1
The Effect of BMS-986195 Combined With an Oral Contraceptive (Ethinyl Estradiol/Norethindrone) in Healthy Female Patients
A Phase 1 study, sponsored by Bristol-Myers Squibb.
- Completed
- Registry status
- Phase 1
- Development phase
- 58
- Enrollment target
NCT03262740: Completed Phase 1 study, sponsored by Bristol-Myers Squibb.
NCT03262740 is a Phase 1 study that has completed, run by Bristol-Myers Squibb. The registered enrollment target is 58 participants, roughly in line with the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT03262740, a Phase 1 study, has completed, sponsored by Bristol-Myers Squibb.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 58 participants
- Enrollment target
Study Summary
The purpose of this study is to investigate the effect of BMS-986195 in combination with an oral contraceptive in healthy female patients.
Interventions
- DRUG BMS-986195
- DRUG Loestrin 1.5/30 (1.5 mg norethindrone acetate/30 μg ethinyl estradiol)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 58 participants |
| Start Date | 2017-09-11 |
| Est. Completion | 2018-01-30 |
| Phase | Phase 1 |
What the finished NCT03262740 record still lists
NCT03262740 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 58 participants, a relatively small participant target, roughly in line with the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target.
The record links to 0 conditions, and to 2 interventions - of which BMS-986195 is the first listed.
NCT03262740 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT03262740 about?
NCT03262740 is a clinical study titled "The Effect of BMS-986195 Combined With an Oral Contraceptive (Ethinyl Estradiol/Norethindrone) in Healthy Female Patients". The purpose of this study is to investigate the effect of BMS-986195 in combination with an oral contraceptive in healthy female patients.
What is the current status of trial NCT03262740?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 58 participants. The study started on 2017-09-11. Estimated completion is 2018-01-30.
What interventions are being tested in trial NCT03262740?
The interventions under investigation include: BMS-986195 (DRUG), Loestrin 1.5/30 (1.5 mg norethindrone acetate/30 μg ethinyl estradiol) (DRUG).
Who is sponsoring clinical trial NCT03262740?
This trial is sponsored by Bristol-Myers Squibb, which has 1,025 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT03262740's enrollment target sits among peer trials
58 895th of 2000 higher than 1,100 of 2,000 other Phase 1 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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