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Completed Phase 2 Interventional Results available

Trial of Eribulin in Patients Who Do Not Achieve Pathologic Complete Response (pCR) Following Neoadjuvant Chemotherapy

ClinicalTrials.gov ID: NCT01401959

Public ClinicalTrials.gov record NCT01401959. 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 27, 2026, 1:21 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Phase II Trial of Eribulin in Patients Who Do Not Achieve Pathologic Complete Response (pCR) Following Neoadjuvant Chemotherapy

Brief summary

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

The investigators propose to evaluate eribulin as adjuvant therapy in breast cancer patients who have residual invasive disease in breast or lymph node tissue following standard neoadjuvant chemotherapy and surgery regimen. Three cohorts of patients will be evaluated separately based on tumor type: triple-negative, hormone-receptor-positive/HER2-negative, and HER2-positive breast cancers.

Study identification

NCT ID
NCT01401959
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
127 participants

Conditions and interventions

Interventions

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
Sep 23, 2011 (Actual)
Primary completion
Apr 3, 2017 (Actual)
Completion
Apr 3, 2017 (Actual)
Last update posted
Jun 15, 2018

2011 – 2017

United States locations

U.S. sites
18
U.S. states
11
U.S. cities
15
Facility City State ZIP Site status
Florida Cancer Specialists North Fort Myers Florida 33916 —
Florida Cancer Specialists South Fort Myers Florida 33916 —
Watson Clinic Center for Cancer Care and Research Lakeland Florida 33805 —
Florida Hospital Cancer Insitute Orlando Florida 32804 —
Northeast Georgia Medical Center Gainesville Georgia 30501 —
Providence Medical Group Terre Haute Indiana 47802 —
Mercy Hospital Portland Maine 04101 —
Center for Cancer and Blood Disorders Bethesda Maryland 20817 —
National Capital Clinical Research Consortium Bethesda Maryland 20817 —
Nebraska Methodist Cancer Center Omaha Nebraska 68114 —
Atlantic Health System Morristown New Jersey 07960 —
Hematology Oncology Associates of Northern NJ Morristown New Jersey 07960 —
Oncology Hematology Care, Inc. Cincinnati Ohio 45242 —
South Carolina Oncology Associates Columbia South Carolina 29210 —
Chattanooga Oncology Hematology Associates Chattanooga Tennessee 37404 —
Tennessee Oncology Nashville Tennessee 37203 —
Texas Health Physician Group Arlington Texas 76011 —
The Center for Cancer and Blood Disorders Fort Worth Texas 76104 —

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 NCT01401959, 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 15, 2018 · Synced Oct 27, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01401959 live on ClinicalTrials.gov.

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