12
Participants
Start Date
December 31, 2009
Primary Completion Date
October 31, 2016
Study Completion Date
October 31, 2016
Chloroquine Standard Dose (500mg/week)
Patients will receive chloroquine (500 mg/once a week) for 1 month prior to surgical removal of the DCIS lesion.
Chloroquine Low Dose (250mg/week)
Patients will receive chloroquine (250 mg/once a week) for 1 month prior to surgical removal of the DCIS lesion.
Breast Biopsy
Patients diagnosed with DCIS will undergo a breast biopsy prior to the start of study treatment. This biopsy is entirely voluntary and is not required to remain in the study. The biopsy will allow researchers to study the tissue for biomarkers and to determine how the DCIS tissue changes during treatment. Additional samples of the DCIS tissue will be collected at the time of surgery.
Medical Oncology and Hematology Associates of Northern Virginia, Fairfax
Virginia Cancer Specialists, PC, Fairfax
Virginia Surgery Associates, Fairfax
Inova Fairfax Hospital, Falls Church
Lead Sponsor
George Mason University
OTHER
University of Pittsburgh Medical Center
OTHER
United States Department of Defense
FED
U.S. Army Medical Research and Development Command
FED
Inova Health Care Services
OTHER