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NCT00267696 · ClinicalTrials.gov registry record · Phase 2

Study of Gemcitabine/Carboplatin/Bevacizumab to Treat Ovarian, Fallopian Tube or Primary Peritoneal Cancer

A Phase 2 study, sponsored by Ohio State University Comprehensive Cancer Center.

Completed
Registry status
Phase 2
Development phase
45
Enrollment target

NCT00267696 is a Phase 2 study that has completed, run by Ohio State University Comprehensive Cancer Center. The registered enrollment target is 45 participants.

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The verdict

NCT00267696, a Phase 2 study, has completed, sponsored by Ohio State University Comprehensive Cancer Center.

COMPLETED
Registry status
Phase 2
Development phase
45 participants
Enrollment target

Study Summary

The purpose of this study is to test the effectiveness, safety and tolerability of the drug combination: gemcitabine, carboplatin and bevacizumab in patients that have been diagnosed with platinum sensitive recurrent ovarian cancer, fallopian tube or primary peritoneal cancer.

Interventions

  • DRUG Bevacizumab
  • DRUG Carboplatin
  • DRUG Gemcitabine

Trial Details

FieldValue
Enrollment Target 45 participants
Start Date 2005-11
Est. Completion 2013-12
Phase Phase 2

What the Registry Record Tells You About NCT00267696

The ClinicalTrials.gov registry entry for NCT00267696 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 45 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Ohio State University Comprehensive Cancer Center, which has 341 total studies on file at ClinicalTrials.gov.

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

NCT00267696 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00267696 about?

NCT00267696 is a clinical study titled "Study of Gemcitabine/Carboplatin/Bevacizumab to Treat Ovarian, Fallopian Tube or Primary Peritoneal Cancer". The purpose of this study is to test the effectiveness, safety and tolerability of the drug combination: gemcitabine, carboplatin and bevacizumab in patients that have been diagnosed with platinum sensitive recurrent ovarian cancer, fallopian tube or primary peritoneal cancer.

What is the current status of trial NCT00267696?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 45 participants. The study started on 2005-11. Estimated completion is 2013-12.

What interventions are being tested in trial NCT00267696?

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

Who is sponsoring clinical trial NCT00267696?

This trial is sponsored by Ohio State University Comprehensive Cancer Center, which has 341 total clinical trials registered on ClinicalTrials.gov.

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

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.