Effects of Maraviroc (MVC) on HIV-related Kaposi's Sarcoma (KS)

PHASE2CompletedINTERVENTIONAL
Enrollment

13

Participants

Timeline

Start Date

March 9, 2011

Primary Completion Date

January 31, 2015

Study Completion Date

April 30, 2015

Conditions
Kaposi's Sarcoma
Interventions
DRUG

Maraviroc

"FDA Recommended dosing will be used in this study. Subjects on an efavirenz or etravirine-based regimen will be dosed at 600 mg orally, twice per day, for 96 weeks.~Subjects on a ritonavir-boosted protease inhibitor based regimen (except for tipranavir/ritonavir) will be dosed at 150 mg orally, twice per day, for 96 weeks.~Subjects that are on regimens that do not include etravirine, efavirenz, or ritonavir will be dosed at 300mg orally, twice per day, for 96 weeks. These doses are based on the recommendations from the company based on drug-drug interactions."

Trial Locations (1)

94110

San Francisco General Hospital, Clinical Trials Unit, San Francisco

Sponsors

Collaborators (2)

All Listed Sponsors
collaborator

Pfizer

INDUSTRY

collaborator

ViiV Healthcare

INDUSTRY

lead

University of California, San Francisco

OTHER