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NCT01420081 · ClinicalTrials.gov registry record · Phase 2

A Study Of Two Dual PI3K/mTOR Inhibitors, PF-04691502 And PF-05212384 In Patients With Recurrent Endometrial Cancer

A Phase 2 study, sponsored by Pfizer.

Terminated
Registry status
Phase 2
Development phase
67
Enrollment target

NCT01420081: Clinical Trial Phase 2 study, sponsored by Pfizer.

NCT01420081 is a Phase 2 study that was terminated before completion, run by Pfizer. The registered enrollment target is 67 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (50% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01420081, a Phase 2 study, was terminated before completion, sponsored by Pfizer.

TERMINATED
Registry status
Phase 2
Development phase
67 participants
Enrollment target

Study Summary

This study will investigate the individual safety and efficacy of two dual PI3K/mTOR inhibitors in patients with recurrent endometrial cancer.

Primary Outcome

Clinical benefit response was defined as best overall response of complete response (CR), partial response (PR) or stable disease (SD) for at least 16 weeks from Cycle 1 Day 1 (C1D1) to the first time of disease progression. The outcome data table below presents the number of participants with clinical benefit response as "yes" or "no". On 09 Oct 2012, Pfizer decided to stop enrollment into PF-04691502. While tumor assessment for PF-04691502 was included as a listing in the final report, formal

Interventions

  • DRUG PF-05212384

Trial Details

FieldValue
Enrollment Target 67 participants
Start Date 2012-01-19
Est. Completion 2015-12-25
Phase Phase 2
Pfizer

1,845 total trials

Why NCT01420081 stopped before completion

NCT01420081 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 67 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (50% lower).

The record links to 0 conditions, and to 1 intervention - of which PF-05212384 is the first listed.

NCT01420081 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01420081 about?

NCT01420081 is a clinical study titled "A Study Of Two Dual PI3K/mTOR Inhibitors, PF-04691502 And PF-05212384 In Patients With Recurrent Endometrial Cancer". This study will investigate the individual safety and efficacy of two dual PI3K/mTOR inhibitors in patients with recurrent endometrial cancer.

What is the current status of trial NCT01420081?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 67 participants. The study started on 2012-01-19. Estimated completion is 2015-12-25.

What interventions are being tested in trial NCT01420081?

The interventions under investigation include: PF-05212384 (DRUG).

Who is sponsoring clinical trial NCT01420081?

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 NCT01420081's enrollment target sits among peer trials

67 974th of 2000 higher than 1,026 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT01420081, the US trial registry maintained by the National Library of Medicine. NCT01420081 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.