Cisplatin vs. Doxorubicin/Cyclophosphamide in BrCa

PHASE2CompletedINTERVENTIONAL
Enrollment

118

Participants

Timeline

Start Date

October 31, 2012

Primary Completion Date

May 31, 2019

Study Completion Date

April 1, 2025

Conditions
Breast Cancer
Interventions
DRUG

Cisplatin

administered intravenously every 3 weeks for 4 doses

DRUG

Cyclophosphamide

administered with doxorubicin intravenously every 2 or 3 weeks for 4 doses

DRUG

Doxorubicin

administered with Cyclophosphamide intravenously every 2 or 3 weeks for 4 doses

Trial Locations (15)

20007

Georgetown University Medical Center, Washington D.C.

21287

Johns Hopkins, Baltimore

27708

Duke University, Durham

77030

MD Anderson Cancer Center, Houston

80045

University of Colorado Cancer Center, Aurora

06418

Smilow Cancer Hospital Care Center at Derby, Derby

06437

Smilow Cancer Hospital Care Center at Guilford, Guilford

06105

St. Francis Hospital and Medical Center, Hartford

06520

Yale School of Medicine, New Haven

20016-2698

Sibley Memorial Hospital, Washington D.C.

02114

Massachusetts General Hospital, Boston

02215

Beth Israel Deaconess Medical Center, Boston

Dana-Farber Cancer Institute, Boston

08901

Rutgers Cancer Institute of New Jersey, New Brunswick

02905

Women and Infants Hospital, Providence

All Listed Sponsors
collaborator

Dana-Farber Cancer Institute

OTHER

lead

Beth Israel Deaconess Medical Center

OTHER

NCT01670500 - Cisplatin vs. Doxorubicin/Cyclophosphamide in BrCa | Biotech Hunter | Biotech Hunter