Title
Pilot Assessment of Lopinavir/Ritonavir and Maraviroc
Pilot Assessment of Lopinavir/Ritonavir and Maraviroc in Experienced Patients
Phase
Phase 4Lead Sponsor
Rodwick, Barry M., M.D.Study Type
InterventionalStatus
TerminatedIndication/Condition
HIV Infections Acquired Immunodeficiency SyndromeStudy Participants
3This is a study to assess the response of lopinavir/ritonavir plus maraviroc (with no nucleoside medications) in HIV patients failing their initial antiviral therapy.
As long-term toxicity to many of the nucleoside medications have become known, interest has increased in treatment regimens that do not use these medications. This study is to assess the response of one such "nucleoside-sparing" therapy in patients who are showing failure to their initial nucleoside-containing treatment regimen.
lopinavir/ritonavir 400/100 mg bid plus maraviroc 150 mg bid
single arm
Inclusion Criteria: HIV viral load > 1,000 on current antiviral medications No resistance to study medications Over 18 years of age Exclusion Criteria: Hepatitis B co-infection Pregnancy Previous therapy with either of the study medications Ongoing substance abuse Significant history of other physical disease