CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 18 enrolled
Drug / intervention
Maraviroc +3 moredrug
Likely dose
Maraviroc 300 milligramsfrom 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/NCT00666705
NCT00666705Phase 4Completed

An Open Label Phase 4 Study To Evaluate An Interaction Between Maraviroc And Raltegravir In Healthy Subjects

ViiV Healthcare·interventional·Posted Apr 25, 2008·Updated Jan 25, 2013

In Brief

A Phase 4 clinical trial evaluating Maraviroc and Raltegravir for Healthy. Completed, enrolled 18 participants across 1 site.

Detailed Summary

An open label study to evaluate an interaction between maraviroc and raltegravir in healthy subjects.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHealthy
CountriesUnited States
CollaboratorsPfizer

Timeline

Phase 4CompletedFinished
20082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedApr 25, 2008
Enrollment StartFeb 1, 2008
Primary CompletionMar 1, 2008
TodayJul 2, 2026
Enrollment to primary: 1 monthPosted 18.2 years ago

Interventions

Maravirocdrug

300 milligrams(mg) every 12 hours Days 6-11

Maravirocdrug

Days 12-14: Raltegravir 400 milligrams(mg) every 12 hours, maraviroc 300 milligrams(mg) every 12 hours (AM doses only on Day 14)

Raltegravirdrug

Days 12-14: Raltegravir 400 milligrams(mg) every 12 hours, maraviroc 300 milligrams(mg) every 12 hours (AM doses only on Day 14)

Raltegravirdrug

400 milligrams(mg) every 12 hours Days 1-3 Followed by washout Days 4-5