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NCT01168232 · ClinicalTrials.gov registry record · Phase 2

Ixabepilone in Treating Patients With Recurrent or Persistent Uterine Cancer

A Phase 2 study, sponsored by National Cancer Institute (NCI).

Completed
Registry status
Phase 2
Development phase
42
Enrollment target

NCT01168232: Completed Phase 2 study, sponsored by National Cancer Institute (NCI).

NCT01168232 is a Phase 2 study that has completed, run by National Cancer Institute (NCI). The registered enrollment target is 42 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (68% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT01168232, a Phase 2 study, has completed, sponsored by National Cancer Institute (NCI).

COMPLETED
Registry status
Phase 2
Development phase
42 participants
Enrollment target

Study Summary

This phase II trial is studying the side effects and how well ixabepilone works in treating patients with persistent or recurrent uterine cancer. Drugs used in chemotherapy, such as ixabepilone, work in different ways to stop the growth of tumor cells, either by killing the cells of by stopping them from dividing.

Primary Outcome

Proportion of participants with objective tumor response. Objective tumor response is defined as complete or partial tumor response as assessed by RECIST 1.1.

Interventions

  • OTHER Laboratory Biomarker Analysis
  • DRUG Ixabepilone

Trial Details

FieldValue
Enrollment Target 42 participants
Start Date 2010-09-07
Est. Completion 2013-11-26
Phase Phase 2
National Cancer Institute (NCI)

3,257 total trials

What the finished NCT01168232 record still lists

NCT01168232 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 42 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (68% lower).

The record links to 0 conditions, and to 2 interventions - of which Laboratory Biomarker Analysis is the first listed.

NCT01168232 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01168232 about?

NCT01168232 is a clinical study titled "Ixabepilone in Treating Patients With Recurrent or Persistent Uterine Cancer". This phase II trial is studying the side effects and how well ixabepilone works in treating patients with persistent or recurrent uterine cancer. Drugs used in chemotherapy, such as ixabepilone, work in different ways to stop the growth of tumor cells, either by killing the cells of by stopping them...

What is the current status of trial NCT01168232?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 42 participants. The study started on 2010-09-07. Estimated completion is 2013-11-26.

What interventions are being tested in trial NCT01168232?

The interventions under investigation include: Laboratory Biomarker Analysis (OTHER), Ixabepilone (DRUG).

Who is sponsoring clinical trial NCT01168232?

This trial is sponsored by National Cancer Institute (NCI), which has 3,257 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01168232's enrollment target sits among peer trials

42 1339th of 2000 higher than 649 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 NCT01168232, the US trial registry maintained by the National Library of Medicine. NCT01168232 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.