Overview

A Study of Valacyclovir to Suppress HSV and HIV Shedding in Coinfected Persons

Status:
Completed
Trial end date:
2006-06-01
Target enrollment:
0
Participant gender:
Male
Summary
The primary objective of this research study is to assess if daily valacyclovir therapy for suppression of HSV-2 reactivation is associated with a decrease in mucosal HIV shedding in individuals co-infected with both HSV-2 and HIV.
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
University of Washington
Collaborators:
GlaxoSmithKline
National Institutes of Health (NIH)
Treatments:
Acyclovir
Valacyclovir
Criteria
Inclusion Criteria:

- HIV seropositive and HSV-2 seropositive

- MSM (men having sex with men)

- 18 years old or older

Exclusion Criteria:

- Known history of adverse reaction to acyclovir or valacyclovir

- Planned open label use of acyclovir, valacyclovir or famciclovir