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NCT00866723 · ClinicalTrials.gov registry record · Phase 2

Avastin in Patients With Epithelial Ovarian, Primary Peritoneal Serous or Fallopian Tube Cancer

A Phase 2 study, sponsored by Beth Israel Deaconess Medical Center.

Terminated
Registry status
Phase 2
Development phase
5
Enrollment target

NCT00866723 is a Phase 2 study that was terminated before completion, run by Beth Israel Deaconess Medical Center. The registered enrollment target is 5 participants.

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The verdict

NCT00866723, a Phase 2 study, was terminated before completion, sponsored by Beth Israel Deaconess Medical Center.

TERMINATED
Registry status
Phase 2
Development phase
5 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate how the participant's disease (ovarian, primary peritoneal serous, fallopian tube, or papillary serous endometrial cancer) responds to additional treatment with Avastin (bevacizumab). Participants have already received Avastin as part of maintenance therapy for their cancer. Maintenance therapy is a medical therapy that is given to people to prevent a relapse. However, cancer may return after maintenance therapy. This research study hopes to determine whether additional treatment with Avastin will be effective in treating the participant's cancer.

Interventions

  • DRUG bevacizumab

Trial Details

FieldValue
Enrollment Target 5 participants
Start Date 2009-03
Est. Completion 2012-06
Phase Phase 2

What the Registry Record Tells You About NCT00866723

The ClinicalTrials.gov registry entry for NCT00866723 describes a study currently listed as terminated, categorized as Phase 2. The registered enrollment target is 5 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Beth Israel Deaconess Medical Center, which has 488 total studies on file at ClinicalTrials.gov.

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

NCT00866723 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00866723 about?

NCT00866723 is a clinical study titled "Avastin in Patients With Epithelial Ovarian, Primary Peritoneal Serous or Fallopian Tube Cancer". The purpose of this study is to evaluate how the participant's disease (ovarian, primary peritoneal serous, fallopian tube, or papillary serous endometrial cancer) responds to additional treatment with Avastin (bevacizumab). Participants have already received Avastin as part of maintenance therapy f...

What is the current status of trial NCT00866723?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 5 participants. The study started on 2009-03. Estimated completion is 2012-06.

What interventions are being tested in trial NCT00866723?

The interventions under investigation include: bevacizumab (DRUG).

Who is sponsoring clinical trial NCT00866723?

This trial is sponsored by Beth Israel Deaconess Medical Center, which has 488 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.