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Active, not recruiting Phase 2 Interventional Results available

Temozolomide With or Without Veliparib in Treating Patients With Relapsed or Refractory Small Cell Lung Cancer

ClinicalTrials.gov ID: NCT01638546

Public ClinicalTrials.gov record NCT01638546. 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 Sep 6, 2026, 4:32 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 Multi-Center, Randomized, Double-Blind Phase II Study Comparing ABT-888, a PARP Inhibitor, Versus Placebo With Temozolomide in Patients With Relapsed Sensitive or Refractory Small Cell Lung Cancer

Brief summary

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

This randomized phase II trial studies how well temozolomide with or without veliparib works in treating patients with small cell lung cancer that has returned or does not respond to treatment. Temozolomide works by damaging molecules inside the cancer cells, such as deoxyribonucleic acid (DNA), that are needed for cancer survival and growth. Veliparib may stop the growth of tumor cells by blocking proteins that are needed for repairing the damaged DNA and it may also help temozolomide to kill more cancer cells. It is not yet know whether temozolomide is more effective with or without veliparib in treating patients with relapsed or refractory small cell lung cancer.

Study identification

NCT ID
NCT01638546
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 2
Enrollment
97 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
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
Jul 26, 2012
Primary completion
Jan 8, 2017
Completion
Mar 24, 2027
Last update posted
Jun 16, 2026

2012 – 2027

United States locations

U.S. sites
14
U.S. states
10
U.S. cities
13
Facility City State ZIP Site status
Moffitt Cancer Center Tampa Florida 33612
Emory University Hospital/Winship Cancer Institute Atlanta Georgia 30322
Johns Hopkins Bayview Medical Center Baltimore Maryland 21224
Johns Hopkins University/Sidney Kimmel Cancer Center Baltimore Maryland 21287
Washington University School of Medicine St Louis Missouri 63110
Memorial Sloan Kettering Basking Ridge Basking Ridge New Jersey 07920
Memorial Sloan Kettering Commack Commack New York 11725
Memorial Sloan Kettering Cancer Center New York New York 10065
Memorial Sloan Kettering Sleepy Hollow Sleepy Hollow New York 10591
Memorial Sloan Kettering Nassau Uniondale New York 11553
UNC Lineberger Comprehensive Cancer Center Chapel Hill North Carolina 27599
Case Western Reserve University Cleveland Ohio 44106
UT MD Anderson Cancer Center Houston Texas 77030
VCU Massey Comprehensive Cancer Center Richmond Virginia 23298

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 NCT01638546, 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 Jun 16, 2026 · Synced Sep 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01638546 live on ClinicalTrials.gov.

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