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Completed Phase 1 Interventional

Carboplatin, Paclitaxel, Bevacizumab, and Veliparib in Treating Patients With Newly Diagnosed Stage II-IV Ovarian Epithelial, Fallopian Tube, or Primary Peritoneal Cancer

ClinicalTrials.gov ID: NCT00989651

Public ClinicalTrials.gov record NCT00989651. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 1:05 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase I Study of Intravenous Carboplatin/Paclitaxel or Intravenous and Intraperitoneal Paclitaxel/Cisplatin in Combination With Continuous or Intermittent /CTEP-Supplied Agent ABT-888 (NSC #737664) and CTEP-Supplied Agent Bevacizumab (NSC #704865) in Newly Diagnosed Patients With Previously Untreated Epithelial Ovarian, Fallopian Tube or Primary Peritoneal Cancer

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This phase I trial studies the side effects and best dose of veliparib when given together with carboplatin, paclitaxel, and bevacizumab in treating patients with newly diagnosed stage II-IV ovarian epithelial, fallopian tube, or primary peritoneal cancer. Veliparib may stop the growth of tumor cells by blocking some of the enzymes needed for cells to repair themselves from damage and survive. Drugs used in chemotherapy, such as carboplatin and paclitaxel, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Bevacizumab, a type of drug called a monoclonal antibody, blocks tumor growth by targeting certain cells and preventing the growth of new blood vessels that tumors need to grow. Giving veliparib together with carboplatin, paclitaxel, and bevacizumab may kill more tumor cells.

Study identification

NCT ID
NCT00989651
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Enrollment
431 participants

Conditions and interventions

Conditions

Interventions

Biological · Drug · Other

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 28, 2009 (Actual)
Primary completion
Sep 2, 2016 (Actual)
Completion
Apr 10, 2020 (Actual)
Last update posted
Oct 20, 2021

2009 – 2020

United States locations

U.S. sites
23
U.S. states
14
U.S. cities
18
Facility City State ZIP Site status
University of Alabama at Birmingham Cancer Center Birmingham Alabama 35233 —
University of Colorado Hospital Aurora Colorado 80045 —
Augusta University Medical Center Augusta Georgia 30912 —
University of Chicago Comprehensive Cancer Center Chicago Illinois 60637 —
University of Iowa/Holden Comprehensive Cancer Center Iowa City Iowa 52242 —
MedStar Franklin Square Medical Center/Weinberg Cancer Institute Baltimore Maryland 21237 —
Johns Hopkins University/Sidney Kimmel Cancer Center Baltimore Maryland 21287 —
Washington University School of Medicine St Louis Missouri 63110 —
Roswell Park Cancer Institute Buffalo New York 14263 —
Memorial Sloan Kettering Cancer Center New York New York 10065 —
Case Western Reserve University Cleveland Ohio 44106 —
MetroHealth Medical Center Cleveland Ohio 44109 —
Cleveland Clinic Cancer Center/Fairview Hospital Cleveland Ohio 44111 —
Cleveland Clinic Foundation Cleveland Ohio 44195 —
Ohio State University Comprehensive Cancer Center Columbus Ohio 43210 —
Riverside Methodist Hospital Columbus Ohio 43214 —
Hillcrest Hospital Cancer Center Mayfield Heights Ohio 44124 —
University of Oklahoma Health Sciences Center Oklahoma City Oklahoma 73104 —
Fox Chase Cancer Center Philadelphia Pennsylvania 19111 —
Women and Infants Hospital Providence Rhode Island 02905 —
University of Virginia Cancer Center Charlottesville Virginia 22908 —
Virginia Commonwealth University/Massey Cancer Center Richmond Virginia 23298 —
University of Wisconsin Hospital and Clinics Madison Wisconsin 53792 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00989651, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 20, 2021 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00989651 live on ClinicalTrials.gov.

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