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

PHASE2CompletedINTERVENTIONAL
Enrollment

127

Participants

Timeline

Start Date

September 23, 2011

Primary Completion Date

April 3, 2017

Study Completion Date

April 3, 2017

Conditions
Metastatic Breast Cancer
Interventions
DRUG

Eribulin

1.4 mg/m\^2 IV Days 1 and 8, every 21 days for six cycles

DRUG

Trastuzumab

6 mg/kg IV Day 1 every 21 days

Trial Locations (18)

20817

Center for Cancer and Blood Disorders, Bethesda

National Capital Clinical Research Consortium, Bethesda

29210

South Carolina Oncology Associates, Columbia

30501

Northeast Georgia Medical Center, Gainesville

32804

Florida Hospital Cancer Insitute, Orlando

33805

Watson Clinic Center for Cancer Care and Research, Lakeland

33916

Florida Cancer Specialists North, Fort Myers

Florida Cancer Specialists South, Fort Myers

37203

Tennessee Oncology, Nashville

37404

Chattanooga Oncology Hematology Associates, Chattanooga

45242

Oncology Hematology Care, Inc., Cincinnati

47802

Providence Medical Group, Terre Haute

68114

Nebraska Methodist Cancer Center, Omaha

76011

Texas Health Physician Group, Arlington

76104

The Center for Cancer and Blood Disorders, Fort Worth

04101

Mercy Hospital, Portland

07960

Atlantic Health System, Morristown

Hematology Oncology Associates of Northern NJ, Morristown

All Listed Sponsors
collaborator

Eisai Inc.

INDUSTRY

lead

SCRI Development Innovations, LLC

OTHER

NCT01401959 - Trial of Eribulin in Patients Who Do Not Achieve Pathologic Complete Response (pCR) Following Neoadjuvant Chemotherapy | Biotech Hunter | Biotech Hunter