Study of the Efficacy of Chloroquine in the Treatment of Ductal Carcinoma in Situ (The PINC Trial)

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

12

Participants

Timeline

Start Date

December 31, 2009

Primary Completion Date

October 31, 2016

Study Completion Date

October 31, 2016

Conditions
Carcinoma, Intraductal, NoninfiltratingDCISDuctal Carcinoma In Situ
Interventions
DRUG

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.

DRUG

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.

PROCEDURE

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.

Trial Locations (4)

22031

Medical Oncology and Hematology Associates of Northern Virginia, Fairfax

Virginia Cancer Specialists, PC, Fairfax

22033

Virginia Surgery Associates, Fairfax

22042

Inova Fairfax Hospital, Falls Church

Sponsors
All Listed Sponsors
collaborator

George Mason University

OTHER

collaborator

University of Pittsburgh Medical Center

OTHER

collaborator

United States Department of Defense

FED

collaborator

U.S. Army Medical Research and Development Command

FED

lead

Inova Health Care Services

OTHER