22
Participants
Start Date
January 1, 2015
Primary Completion Date
April 30, 2017
Study Completion Date
September 30, 2017
Maraviroc 300 mg
Patients were randomly allocated with an AB/BA cross over design to either maraviroc 300 mg/day to current ART for 24 weeks (A) or no additional treatment (B). At the end of the first 24-week period patients were switched to the alternative arm.
Elisabetta Schiaroli, Perugia
University Of Perugia
OTHER