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NCT01063023 · ClinicalTrials.gov registry record · Phase 1

Drug Interaction Oral Contraceptive Pill (OCP)

A Phase 1 study, sponsored by Bristol-Myers Squibb.

Completed
Registry status
Phase 1
Development phase
20
Enrollment target

NCT01063023: Completed Phase 1 study, sponsored by Bristol-Myers Squibb.

NCT01063023 is a Phase 1 study that has completed, run by Bristol-Myers Squibb. The registered enrollment target is 20 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (67% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01063023, a Phase 1 study, has completed, sponsored by Bristol-Myers Squibb.

COMPLETED
Registry status
Phase 1
Development phase
20 participants
Enrollment target

Study Summary

To assess the effects of BMS-650032 on Pharmacokinetics (PK) of ethinyl estradiol (EE) and norelgestromin (NGMN) in healthy female subjects

Interventions

  • DRUG Ortho Tri-Cyclen®
  • DRUG BMS-650032

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2010-01
Est. Completion 2010-06
Phase Phase 1
Bristol-Myers Squibb

1,025 total trials

What the finished NCT01063023 record still lists

NCT01063023 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (67% lower).

The record links to 0 conditions, and to 2 interventions - of which Ortho Tri-Cyclen® is the first listed.

NCT01063023 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01063023 about?

NCT01063023 is a clinical study titled "Drug Interaction Oral Contraceptive Pill (OCP)". To assess the effects of BMS-650032 on Pharmacokinetics (PK) of ethinyl estradiol (EE) and norelgestromin (NGMN) in healthy female subjects

What is the current status of trial NCT01063023?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 20 participants. The study started on 2010-01. Estimated completion is 2010-06.

What interventions are being tested in trial NCT01063023?

The interventions under investigation include: Ortho Tri-Cyclen® (DRUG), BMS-650032 (DRUG).

Who is sponsoring clinical trial NCT01063023?

This trial is sponsored by Bristol-Myers Squibb, which has 1,025 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01063023's enrollment target sits among peer trials

20 1629th of 2000 higher than 285 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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Source: ClinicalTrials.gov NCT01063023, the US trial registry maintained by the National Library of Medicine. NCT01063023 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.