Study of Hydroxychloroquine and Aldesleukin in Renal Cell Carcinoma Patients (RCC)

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

30

Participants

Timeline

Start Date

March 31, 2012

Primary Completion Date

February 6, 2018

Study Completion Date

February 28, 2019

Conditions
Metastatic Renal Cell Carcinoma
Interventions
DRUG

Hydroxychloroquine

Continuous oral administration (at 600 mg/d) will be initiated prior to the first dose (day -14) given 14 days prior to initiation of the first dose of IL-2 and then daily or twice a day throughout all three treatment courses.

DRUG

IL-2

600,000 IU/kg IV bolus q 8 hrs x days 1-5 and 15-19 (maximum 28 doses - 14 per 5 day cycle) of each 84-day course

Trial Locations (7)

15232

University of Pittsburgh Cancer Institute / UPMC CancerCenter, Pittsburgh

43210

The Ohio State University Comprehensive Cancer Center, Columbus

46202

Indiana University Simon Cancer Center, Indianapolis

60153

Loyola University Chicago, Maywood

97213

Providence Health & Services, Portland

02215

Dana Farber Cancer Institute, Boston

03755

Dartmouth-Hitchcock Medical Center, Hanover

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Prometheus Laboratories

INDUSTRY

lead

Leonard Appleman

OTHER

NCT01550367 - Study of Hydroxychloroquine and Aldesleukin in Renal Cell Carcinoma Patients (RCC) | Biotech Hunter | Biotech Hunter