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NCT00418093 · ClinicalTrials.gov registry record · Phase 2

Oxaliplatin, Gemcitabine and Bevacizumab in Women With Recurrent Mullerian Carcinoma

A Phase 2 study, sponsored by Dana-Farber Cancer Institute.

Terminated
Registry status
Phase 2
Development phase
19
Enrollment target

NCT00418093: Clinical Trial Phase 2 study, sponsored by Dana-Farber Cancer Institute.

NCT00418093 is a Phase 2 study that was terminated before completion, run by Dana-Farber Cancer Institute. The registered enrollment target is 19 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (86% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00418093, a Phase 2 study, was terminated before completion, sponsored by Dana-Farber Cancer Institute.

TERMINATED
Registry status
Phase 2
Development phase
19 participants
Enrollment target

Study Summary

The main purpose of this study is to begin to collect information and try to learn whether or not the combination of oxaliplatin, gemcitabine and bevacizumab works in treating women with recurrent mullerian carcinoma. We will also collect more information about the safety and side effects of this combination of drugs. Gemcitabine and oxaliplatin are chemotherapy drugs that kill cancer cells. Bevacizumab is a new anti-cancer drug that works to slow or stop cell growth in cancerous tumors by decreasing the blood supply to the tumors.

Primary Outcome

Precentage of women who responded to the treatment regimen Response was determined by RECIST criteria

Interventions

  • DRUG Bevacizumab
  • DRUG Oxaliplatin
  • DRUG Gemcitabine

Trial Details

FieldValue
Enrollment Target 19 participants
Start Date 2006-09
Est. Completion 2011-10
Phase Phase 2
Dana-Farber Cancer Institute

781 total trials

Why NCT00418093 stopped before completion

NCT00418093 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 19 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (86% lower).

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

NCT00418093 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00418093 about?

NCT00418093 is a clinical study titled "Oxaliplatin, Gemcitabine and Bevacizumab in Women With Recurrent Mullerian Carcinoma". The main purpose of this study is to begin to collect information and try to learn whether or not the combination of oxaliplatin, gemcitabine and bevacizumab works in treating women with recurrent mullerian carcinoma. We will also collect more information about the safety and side effects of this co...

What is the current status of trial NCT00418093?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 19 participants. The study started on 2006-09. Estimated completion is 2011-10.

What interventions are being tested in trial NCT00418093?

The interventions under investigation include: Bevacizumab (DRUG), Oxaliplatin (DRUG), Gemcitabine (DRUG).

Who is sponsoring clinical trial NCT00418093?

This trial is sponsored by Dana-Farber Cancer Institute, which has 781 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00418093's enrollment target sits among peer trials

19 1894th of 2000 higher than 103 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 NCT00418093, the US trial registry maintained by the National Library of Medicine. NCT00418093 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.