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A Phase 1 Pharmacokinetic Study to Assess the Steady State Pharmacokinetic Profile and Short Term Safety of Maraviroc Dosed With Darunavir/Ritonavir All Once Daily, With and Without Nucleoside Analogues, in HIV-1 Infected Subjects
This is a phase I, open label, prospective, two phase pharmacokinetic study. Subjects currently attending for HIV care at St. Mary's Hospital, London will be eligible.
Details
| Lead sponsor | Imperial College London |
|---|---|
| Phase | Phase 1 |
| Status | COMPLETED |
| Enrolment | 13 |
| Start date | 2011-10 |
| Completion | 2012-05 |
Conditions
- HIV
Interventions
- Maraviroc
- Truvada
- Darunavir
Primary outcomes
- The Ratio of the Maximum Plasma Concentration of Maraviroc Between 20 and 10 Day — 10 day, 20 days
On day 10 of the study the maximum concentractions of maraviroc will be measured . On day 20 of the study the maximum plasma concentractions maraviroc will be measured .
Countries
United Kingdom