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NCT04018274 · ClinicalTrials.gov registry record · Phase 1

Effect of PF-06651600 on the Pharmacokinetics of Oral Contraceptive Steroids

A Phase 1 study, sponsored by Pfizer.

Completed
Registry status
Phase 1
Development phase
29
Enrollment target

NCT04018274: Completed Phase 1 study, sponsored by Pfizer.

NCT04018274 is a Phase 1 study that has completed, run by Pfizer. The registered enrollment target is 29 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (52% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04018274, a Phase 1 study, has completed, sponsored by Pfizer.

COMPLETED
Registry status
Phase 1
Development phase
29 participants
Enrollment target

Study Summary

This is a Phase 1, randomized, 2 way crossover, open-label study of the effect of multiple-dose PF 06651600 on single-dose oral contraceptive (OC) pharmacokinetics (PK) in healthy female subjects. Subjects will be randomized to 1 of 2 treatment sequences. A total of 28 healthy female subjects (14 in each treatment sequence) will be enrolled in the study. Each treatment sequence will consist of 2 periods.

Primary Outcome

30 micrograms administered as oral OC combination tablet

Interventions

  • DRUG PF-06651600
  • DRUG Ethinyl estradiol (EE) and levonorgestrel(LN)

Trial Details

FieldValue
Enrollment Target 29 participants
Start Date 2019-08-09
Est. Completion 2019-10-16
Phase Phase 1
Pfizer

1,845 total trials

What the finished NCT04018274 record still lists

NCT04018274 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 29 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (52% lower).

The record links to 0 conditions, and to 2 interventions - of which PF-06651600 is the first listed.

NCT04018274 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04018274 about?

NCT04018274 is a clinical study titled "Effect of PF-06651600 on the Pharmacokinetics of Oral Contraceptive Steroids". This is a Phase 1, randomized, 2 way crossover, open-label study of the effect of multiple-dose PF 06651600 on single-dose oral contraceptive (OC) pharmacokinetics (PK) in healthy female subjects. Subjects will be randomized to 1 of 2 treatment sequences. A total of 28 healthy female subjects (14 in...

What is the current status of trial NCT04018274?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 29 participants. The study started on 2019-08-09. Estimated completion is 2019-10-16.

What interventions are being tested in trial NCT04018274?

The interventions under investigation include: PF-06651600 (DRUG), Ethinyl estradiol (EE) and levonorgestrel(LN) (DRUG).

Who is sponsoring clinical trial NCT04018274?

This trial is sponsored by Pfizer, which has 1,845 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04018274's enrollment target sits among peer trials

29 1440th of 2000 higher than 554 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 NCT04018274, the US trial registry maintained by the National Library of Medicine. NCT04018274 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.