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Safety and Acceptability Study of Non-occupational Prophylaxis (PEP) Following Potential Exposure to HIV — BMS PEP  

HIV Clinical Trial

Official title:
A Phase IV Open-label Evaluation of Safety, Tolerability and Patient Acceptance of Atazanavir Boosted With Ritonavir Combined With a Fixed-dose Formulation of Tenofovir DF and Emtricitabine for Non-occupational Prophylaxis Following Potential Exposure to HIV-1

Clinical Trial Summary

This study will evaluate how safe and tolerable a combination of taking three-drugs will be for the purpose of preventing HIV transmission after a high-risk sexual contact exposure in HIV uninfected adults.

Clinical Trial Description

Participants are given a regimen containing TDF 300mg and FTC 200mg fixed-dose combination tablet (TDF/FTC) once daily, and atazanavir, one 300mg tablet and one 100 mg ritonavir given once daily,for 28 days. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01602822
Study type Interventional
Source Fenway Community Health
Contact
Status Terminated
Phase Phase 4
Start date February 2012
Completion date May 2012
View Details
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