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Completed Phase 1Phase 2 Interventional Results available

Veliparib and Temozolomide in Treating Patients With Recurrent Glioblastoma

ClinicalTrials.gov ID: NCT01026493

Public ClinicalTrials.gov record NCT01026493. 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 Jul 21, 2026, 7:06 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 Randomized Phase I/II Study of ABT-888 in Combination With Temozolomide in Recurrent (Temozolomide Resistant) Glioblastoma

Study identification

NCT ID
NCT01026493
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Radiation Therapy Oncology Group
Network
Enrollment
257 participants

Conditions and interventions

Interventions

  • temozolomide 60 mg x 21 days Drug
  • temozolomide 75 mg x 21 days Drug
  • ABT-888 20 mg x 21 days Drug
  • ABT-888 40 mg x 21 days Drug
  • Temozolomide 150 mg x 5 days Drug
  • ABT-888 40 mg x 5 days Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 120 Years
Sex
All
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
Jun 30, 2010
Primary completion
Apr 30, 2014
Completion
Nov 30, 2016
Last update posted
Jul 1, 2017

2010 – 2016

United States locations

U.S. sites
17
U.S. states
11
U.S. cities
14
Facility City State ZIP Site status
Rebecca and John Moores UCSD Cancer Center La Jolla California 92093-0658
Cedars-Sinai Medical Center Los Angeles California 90048
Cancer Research Center of Hawaii Honolulu Hawaii 96813
Queen's Cancer Institute at Queen's Medical Center Honolulu Hawaii 96813
Hawaii Medical Center - East Honolulu Hawaii 96817
Leeward Radiation Oncology ‘Ewa Beach Hawaii 96706
University of Chicago Cancer Research Center Chicago Illinois 60637-1470
CCOP - Kansas City Prairie Village Kansas 66208
Central Baptist Hospital Lexington Kentucky 40503-9985
Louisville Oncology at Norton Cancer Institute - Louisville Louisville Kentucky 40202
Regional Cancer Center at Singing River Hospital Pascagoula Mississippi 39581
Renown Institute for Cancer at Renown Regional Medical Center Reno Nevada 89502
Norris Cotton Cancer Center at Dartmouth-Hitchcock Medical Center Lebanon New Hampshire 03756-0002
Cancer Institute of New Jersey at UMDNJ - Robert Wood Johnson Medical School New Brunswick New Jersey 08903
Highland Hospital of Rochester Rochester New York 14620
James P. Wilmot Cancer Center at University of Rochester Medical Center Rochester New York 14642
Legacy Good Samaritan Hospital & Comprehensive Cancer Center Portland Oregon 97210

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 NCT01026493, 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 Jul 1, 2017 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01026493 live on ClinicalTrials.gov.

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