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Completed Phase 2 Interventional

A Trial of ABT-888 in Combination With Temozolomide Versus Pegylated Liposomal Doxorubicin Alone in Ovarian Cancer

ClinicalTrials.gov ID: NCT01113957

Public ClinicalTrials.gov record NCT01113957. 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 2, 2026, 12:50 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 2 Randomized Clinical Trial of ABT-888 in Combination With Temozolomide Versus Pegylated Liposomal Doxorubicin Alone in Subjects With Recurrent High Grade Serous Ovarian Cancer

Brief summary

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

The purpose of this study is to determine the objective response rate of ABT-888 when given in combination with temozolomide versus pegylated liposomal doxorubicin (PLD) alone in subjects with recurrent high grade serous ovarian cancer.

Study identification

NCT ID
NCT01113957
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
AbbVie (prior sponsor, Abbott)
Industry
Enrollment
168 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 99 Years
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
Feb 28, 2010
Primary completion
May 31, 2013
Completion
May 31, 2013
Last update posted
Jun 5, 2018

2010 – 2013

United States locations

U.S. sites
15
U.S. states
9
U.S. cities
15
Facility City State ZIP Site status
Site Reference ID/Investigator# 25028 Duarte California 91010
Site Reference ID/Investigator# 25024 Encino California 91436
Site Reference ID/Investigator# 25034 Los Angeles California 90048
Site Reference ID/Investigator# 25037 Newport Beach California 92663
Site Reference ID/Investigator# 25030 Chicago Illinois 60637-1470
Site Reference ID/Investigator# 27837 Park Ridge Illinois 60068
Site Reference ID/Investigator# 25039 Peoria Illinois 61615-7828
Site Reference ID/Investigator# 25038 Albuquerque New Mexico 87131
Site Reference ID/Investigator# 25023 New York New York 10065
Site Reference ID/Investigator# 25041 Chapel Hill North Carolina 27599-7570
Site Reference ID/Investigator# 25029 Hilliard Ohio 43026
Site Reference ID/Investigator# 25543 Oklahoma City Oklahoma 73104
Site Reference ID/Investigator# 25036 Philadelphia Pennsylvania 19111
Site Reference ID/Investigator# 25042 Pittsburgh Pennsylvania 15213
Site Reference ID/Investigator# 25027 Houston Texas 77030

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 17 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01113957, 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 5, 2018 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01113957 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →