A Demonstration Project to Add Pre- or Post-exposure Prophylaxis to Combination HIV Prevention Services

PHASE4CompletedINTERVENTIONAL
Enrollment

328

Participants

Timeline

Start Date

May 31, 2013

Primary Completion Date

May 31, 2016

Study Completion Date

May 31, 2016

Conditions
HIV Prevention
Interventions
DRUG

emtricitabine 200mg/tenofovir 300mg

The intervention medication will be tenofovir + emtricitabine, provided as a fixed-dose combination tablet as Truvada®. Dosing is 1 tablet by mouth once daily. For participants with a a confirmed (i.e. two consecutive) reduction in creatinine clearance (CrCl) to \<50 mL/min, Truvada will be dose-reduced to 1 tablet by mouth every other day. For patients with CrCl \<30 mL/min, Truvada will be discontinued.

Trial Locations (2)

90028

L.A. Gay and Lesbian Center, Los Angeles

90059

The OASIS Clinic, Los Angeles

All Listed Sponsors
collaborator

Los Angeles County Department of Public Health

OTHER_GOV

collaborator

Los Angeles LGBT Center

OTHER

collaborator

The OASIS Clinic

UNKNOWN

collaborator

AIDS Project Los Angeles

OTHER

lead

University of California, Los Angeles

OTHER

NCT01781806 - A Demonstration Project to Add Pre- or Post-exposure Prophylaxis to Combination HIV Prevention Services | Biotech Hunter | Biotech Hunter