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Completed Phase 2 Interventional Results available

PARP Inhibition for Triple Negative Breast Cancer (ER-/PR-/HER2-)With BRCA1/2 Mutations

ClinicalTrials.gov ID: NCT01074970

Public ClinicalTrials.gov record NCT01074970. 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 18, 2026, 4:12 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

PARP Inhibition After Preoperative Chemotherapy in Patients With Triple Negative Breast Cancer or ER/PR +, HER2 Negative With Known BRCA1/2 Mutations: Hoosier Oncology Group BRE09-146

Brief summary

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

The purpose of this trial is to evaluate 2-year disease-free survival in this patient population treated with single agent cisplatin and patients treated with cisplatin in combination with Rucaparib following preoperative chemotherapy. Side effects and tolerability of this treatment in patients with residual disease following preoperative chemotherapy will also be observed and characterized.

Study identification

NCT ID
NCT01074970
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
135 participants

Conditions and interventions

Conditions

Interventions

Drug

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
Feb 2010 (Type not available)
Primary completion
Dec 15, 2018 (Actual)
Completion
Dec 15, 2018 (Actual)
Last update posted
Sep 19, 2024

2010 – 2018

United States locations

U.S. sites
27
U.S. states
15
U.S. cities
25
Facility City State ZIP Site status
St. Jude Heritage Healthcare Fullerton California 92835 —
University of California Los Angeles Los Angeles California 90095 —
Central Coast Medical Oncology Corporation Santa Maria California 93454 —
University of Colorado Cancer Center Aurora Colorado 80045 —
Memorial Cancer Institute Breast Cancer Center Hollywood Florida 33021 —
University of Miami, Sylvester Comprehensive Cancer Center Miami Florida 33136 —
Fort Wayne Oncology & Hematology, Inc Fort Wayne Indiana 46815 —
Indiana University Melvin and Bren Simon Cancer Center Indianapolis Indiana 46202 —
Community Regional Cancer Center Indianapolis Indiana 46256 —
Horizon Oncology Research, Inc./IU Health Arnett Lafayette Indiana 47905 —
Monroe Medical Associates Munster Indiana 46321 —
Northern Indiana Cancer Research Consortium South Bend Indiana 46601 —
Metro Health Cancer Care Wyoming Michigan 49519 —
Siteman Cancer Center St Louis Missouri 63110 —
Comprehensive Cancer Centers of Nevada Las Vegas Nevada 89128 —
The Center for Cancer & Hematologic Disease Cherry Hill New Jersey 08003 —
Virtua Health Cancer Program Mount Holly New Jersey 08060 —
South Jersey Health Care Vineland New Jersey 08360 —
Presbyterian Medical Group Albuquerque New Mexico 87110 —
University of New Mexico Cancer Center: Albuquerque Albuquerque New Mexico 87131 —
HOPE a Women's Cancer Center Asheville North Carolina 28806 —
Seidman Cancer Center Cleveland Ohio 44106 —
Oregon Health Sciences University Portland Oregon 97239 —
Pinnacle Health Fox Chase Regional Cancer Center Harrisburg Pennsylvania 17110 —
Bux-Mont Oncology Hematology Associates (FCCC) at Grand View Hospital Sellersville Pennsylvania 18960 —
The West Clinic Memphis Tennessee 38138 —
Virginia Oncology Associates Norfolk Virginia 23502 —

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 NCT01074970, 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 Sep 19, 2024 · Synced Oct 18, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01074970 live on ClinicalTrials.gov.

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