CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 13 enrolled
Drug / intervention
Maraviroc +2 moredrug
Likely dose
Maraviroc 150 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01348763
NCT01348763Phase 1Completed

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

Imperial College London·interventional·Posted May 5, 2011·Updated Oct 31, 2019

In Brief

A Phase 1 clinical trial evaluating Maraviroc, Truvada, and 1 other intervention for HIV. Completed, enrolled 13 participants across 1 site.

Detailed Summary

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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHIV
CountriesUnited Kingdom
Collaborators--

Timeline

Phase 1CompletedFinished
2011201220132014201520162017201820192020202120222023202420252026
First PostedMay 5, 2011
Enrollment StartOct 1, 2011
Primary CompletionFeb 1, 2012
Study CompletionMay 1, 2012
TodayJul 2, 2026
Enrollment to primary: 4 monthsPosted 15.2 years ago

Interventions

Maravirocdrug

Maraviroc 150 mg daily

Truvadadrug

daily until 10. day then stop

Darunavirdrug

daily until 10. day then stop