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NCT00945139 · ClinicalTrials.gov registry record · Phase 2

Study of Bevacizumab/Doxil in Treatment of Platinum-Resistant/Refractory Ovarian Cancer (CA)

A Phase 2 study, sponsored by New Mexico Cancer Research Alliance.

Completed
Registry status
Phase 2
Development phase
46
Enrollment target

NCT00945139: Completed Phase 2 study, sponsored by New Mexico Cancer Research Alliance.

NCT00945139 is a Phase 2 study that has completed, run by New Mexico Cancer Research Alliance. The registered enrollment target is 46 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (65% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00945139, a Phase 2 study, has completed, sponsored by New Mexico Cancer Research Alliance.

COMPLETED
Registry status
Phase 2
Development phase
46 participants
Enrollment target

Study Summary

The purpose of this research study is to test the safety, tolerability, and effectiveness of two chemotherapy drugs, pegylated liposomal doxorubicin (Doxil) and bevacizumab (Avastin). How Doxil is metabolized and excreted from the body will also be studied.

Primary Outcome

Tumor response is evaluated according to Response Evaluation Criteria in Solid Tumors (RECIST) (version 1.0). Target lesions are assessed by hysical exam and/or computerized tomography (CT): Complete Response (CR), Disappearance of all target lesions; Partial Response (PR), \>=30% decrease in the sum of the longest diameter of target lesions; Stable Disease (SD), neither sufficient decrease in the sum of the longest diameter of target lesions to qualify for PR nor sufficient increase in the sum

Interventions

  • DRUG Doxil
  • DRUG Avastin

Trial Details

FieldValue
Enrollment Target 46 participants
Start Date 2007-03
Est. Completion 2011-08
Phase Phase 2

What the finished NCT00945139 record still lists

NCT00945139 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 46 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (65% lower).

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

NCT00945139 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00945139 about?

NCT00945139 is a clinical study titled "Study of Bevacizumab/Doxil in Treatment of Platinum-Resistant/Refractory Ovarian Cancer (CA)". The purpose of this research study is to test the safety, tolerability, and effectiveness of two chemotherapy drugs, pegylated liposomal doxorubicin (Doxil) and bevacizumab (Avastin). How Doxil is metabolized and excreted from the body will also be studied.

What is the current status of trial NCT00945139?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 46 participants. The study started on 2007-03. Estimated completion is 2011-08.

What interventions are being tested in trial NCT00945139?

The interventions under investigation include: Doxil (DRUG), Avastin (DRUG).

Who is sponsoring clinical trial NCT00945139?

This trial is sponsored by New Mexico Cancer Research Alliance, which has 66 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00945139's enrollment target sits among peer trials

46 1286th of 2000 higher than 705 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 NCT00945139, the US trial registry maintained by the National Library of Medicine. NCT00945139 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.