30
Participants
Start Date
August 31, 2006
Primary Completion Date
October 31, 2008
Study Completion Date
November 30, 2008
Valganciclovir
900mg PO qd x 8 weeks followed by 4 weeks of observation on background antiretroviral (ARV) regimen alone.
Placebo
Placebo designed to resemble Valganciclovir
San Francisco General Hospital - General Clinical Research Center, San Francisco
Roche Pharma AG
INDUSTRY
University of California, San Francisco
OTHER