drugset / Trial / NCT01114425
Safety Study of Isentress® + Truvada® in Post-exposure Treatment of HIV Infection
Phase 3
Completed
149 enrolled
Groupe d'Etude sur le Risque d'Exposition des Soignants aux Agents Infectieux
Merck Sharp & Dohme LLC · collab
CrossoverOpen-labelTreatment
Summary
The objective are to assess the nature and incidence of drug intolerance observed with a new antiretroviral triple therapy, Truvada® \[0-0-1\] + Isentress® 400 mg tablets \[1-0-1\], prescribed in a setting of the treatment of individuals with recent exposure to a risk of transmission of HIV infection and to compare the results with those of previous studies conducted according to the same methodology, with other combinations of antiretrovirals.
Timeline
- Start
- 2010-11-01
- Primary completion
- 2012-08-01
- Completion
- 2012-12-01
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Raltegravir | Other / unclassified | 400 mg | — |
| Subject | Tenofovir | Small molecule | — | — |