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Completed Phase 2 Interventional Results available

Cisplatin vs Paclitaxel for Triple Negative Breast Cancer

ClinicalTrials.gov ID: NCT01982448

Public ClinicalTrials.gov record NCT01982448. 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 22, 2026, 3:17 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 II Study of Preoperative Cisplatin Versus Paclitaxel in Patients With Triple Negative Breast Cancer: Evaluating the Homologous Recombination Deficiency (HRD) Biomarker

Study identification

NCT ID
NCT01982448
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Dana-Farber Cancer Institute
Other
Enrollment
147 participants

Conditions and interventions

Interventions

  • Cisplatin Drug
  • Paclitaxel Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
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
Mar 31, 2014
Primary completion
Dec 31, 2018
Completion
Jul 31, 2020
Last update posted
Sep 29, 2025

2014 – 2020

United States locations

U.S. sites
20
U.S. states
11
U.S. cities
19
Facility City State ZIP Site status
University of Alabama Birmingham Alabama 35294
Indiana University- Simon Cancer Center Indianapolis Indiana 46202
Johns Hopkins University Baltimore Maryland 21287
Beth Israel Deaconess Medical Center Boston Massachusetts 02215
Dana-Farber Cancer Institute Boston Massachusetts 02215
South Shore Hospital Weymouth Massachusetts 02190
Memorial Sloan Kettering Cancer Center-Basking Ridge Basking Ridge New Jersey 07920
Memorial Sloan Kettering Cancer Center-Monmouth Middletown New Jersey 07748
Memorial Sloan Kettering Cancer Center-Commack Commack New York 11725
Memorial Sloan Kettering Cancer Center-West Harrison Harrison New York 10604
Memorial Sloan Kettering Cancer Center New York New York 10065
Memorial Sloan Kettering Cancer Center-Rockville Centre Rockville Centre New York 11570
Memorial Sloan Kettering Cancer Center-Sleepy Hollow Sleepy Hollow New York 10591
University of North Carolina- Lineberger Cancer Center Chapel Hill North Carolina 27599
Duke University Durham North Carolina 27710
Universtiy of Pittsburgh- Magee-Womens Hospital Pittsburgh Pennsylvania 15213
Vanderbilt-Ingram Cancer Center Nashville Tennessee 37232
Baylor College of Medicine Houston Texas 77030
Seattle Cancer Alliance at EvergreenHealth Kirkland Washington 98034
University of Washignton Seattle Washington 98195

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 NCT01982448, 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 29, 2025 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01982448 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →