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NCT01256268 · ClinicalTrials.gov registry record · Phase 1

Carboplatin/Taxol/Ridaforolimus in Endometrial, Ovarian and Solids

A Phase 1 study, sponsored by H. Lee Moffitt Cancer Center and Research Institute.

Completed
Registry status
Phase 1
Development phase
24
Enrollment target

NCT01256268: Completed Phase 1 study, sponsored by H. Lee Moffitt Cancer Center and Research Institute.

NCT01256268 is a Phase 1 study that has completed, run by H. Lee Moffitt Cancer Center and Research Institute. The registered enrollment target is 24 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (60% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01256268, a Phase 1 study, has completed, sponsored by H. Lee Moffitt Cancer Center and Research Institute.

COMPLETED
Registry status
Phase 1
Development phase
24 participants
Enrollment target

Study Summary

The purpose of this study is to: * Test the safety of a new investigational drug called MK-8669 (ridaforolimus) * Determine the maximum tolerated dose of MK-8669 * Determine the effectiveness of the maximum tolerated dose of MK-8669

Primary Outcome

To determine the maximal tolerated dose of oral ridaforolimus in combination with paclitaxel and carboplatin during the first cycle of treatment.

Interventions

  • DRUG Paclitaxel
  • DRUG carboplatin
  • DRUG Ridaforolimus

Trial Details

FieldValue
Enrollment Target 24 participants
Start Date 2011-06-13
Est. Completion 2017-08-03
Phase Phase 1

What the finished NCT01256268 record still lists

NCT01256268 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 24 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (60% lower).

The record links to 0 conditions, and to 3 interventions - of which Paclitaxel is the first listed.

NCT01256268 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01256268 about?

NCT01256268 is a clinical study titled "Carboplatin/Taxol/Ridaforolimus in Endometrial, Ovarian and Solids". The purpose of this study is to: * Test the safety of a new investigational drug called MK-8669 (ridaforolimus) * Determine the maximum tolerated dose of MK-8669 * Determine the effectiveness of the maximum tolerated dose of MK-8669

What is the current status of trial NCT01256268?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 24 participants. The study started on 2011-06-13. Estimated completion is 2017-08-03.

What interventions are being tested in trial NCT01256268?

The interventions under investigation include: Paclitaxel (DRUG), carboplatin (DRUG), Ridaforolimus (DRUG).

Who is sponsoring clinical trial NCT01256268?

This trial is sponsored by H. Lee Moffitt Cancer Center and Research Institute, which has 502 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01256268's enrollment target sits among peer trials

24 1520th of 2000 higher than 405 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 NCT01256268, the US trial registry maintained by the National Library of Medicine. NCT01256268 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.