GOG-0280
Terminated
Protocol Information
Tab containing protocol details, study design, and eligibility criteria
Tab containing study documents, informed consent forms, and study materials
Tab containing information for potential study participants
A Phase II Evaluation of the Poly (ADP-Ribose) Polymerase (PARP)-1 and -2 Inhibitor Veliparib (ABT-888) (IND#77840) (NSC #737664) in the Treatment of Persistent or Recurrent Epithelial Ovarian, Fallopian Tube, or Primary Peritoneal Cancer Patients Who Carry a Germline BRCA1 or BRCA2 Mutation
Principal Investigator
Robert Coleman
Status
Terminated
Closed to Accrual
November 15, 2012
Closed to Accrual & Treatment
August 28, 2017
Terminated
January 27, 2018
Disease Site
Gynecologic [GY] Ovarian
Phase
II
Developmental Therapeutics
No
Primary Objective
To estimate the proportion of patients who have objective tumor response (complete or partial).
To determine the frequency and severity of adverse events associated with treatment with veliparib (ABT-888) as assessed by the Active Version of the National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) version 4.0.
Patient Population
Patients who have objective tumor response (complete or partial).
Target Accrual
51
Protocol Document
Patient Study Webpage
There is no available patient study webpage available for this trial at this time.