Efficacy of VHM After Treatment Interruption in Subjects Initiating ART During Acute HIV Infection

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

15

Participants

Timeline

Start Date

January 31, 2015

Primary Completion Date

November 30, 2015

Study Completion Date

March 31, 2016

Conditions
Acute HIV Infection
Interventions
DRUG

Vorinostat

Vorinostat (suberoylanilide hydroxamic acid) inhibits histone deacetylases class I and II. Vorinostat is supplied as 100mg capsules and will be administered at 400mg/ day in 2 week cycles beginning at week 0 for 10 weeks - 42 doses.

DRUG

Hydroxychloroquine

Hydroxychloroquine is supplied as 200mg tablets and will be administered at week 0 for 10 weeks

DRUG

Maraviroc

Maraviroc will be administered at 150 to 600mg/ml twice daily depending on the subject's ART regimen at week 0 for 10 weeks

DRUG

Tenofovir

NRTI. Tenofovir will be administered at 300mg 1 X day at week 0 for 10 weeks

DRUG

Emtricitabine

NRTI. Emtricitabine will be administered at 200mg 1 X day at week 0 for 10 weeks

DRUG

Efavirenz

NNRTI. Efavirenz will be administered at 600 mg 1 X day at week 0 for 10 weeks

DRUG

Darunavir

Protease Inhibitor. Darunavir will be administered at a dose of 900mg 1 X day for subjects on NNRTI based ART beginning at week 8 until week 10

Trial Locations (1)

10330

SEARCH, the Thai Red Cross AIDS Research Centre, Bangkok

All Listed Sponsors
collaborator

The Thai Red Cross AIDS Research Centre

UNKNOWN

collaborator

Cooper Human Systems

INDUSTRY

lead

SEARCH Research Foundation

OTHER

NCT02475915 - Efficacy of VHM After Treatment Interruption in Subjects Initiating ART During Acute HIV Infection | Biotech Hunter | Biotech Hunter