The purpose of this study is to determine the effect that telaprevir and boceprevir has on
the pharmacokinetics of maraviroc.
Drug: Maraviroc + Boceprevir
Drug: Maraviroc + Telaprevir
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Locations near you
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Full eligibility criteria for NCT01597895
Ages eligible for Study
18 Years to 55 Years
Genders eligible for Study
Accepts Healthy Volunteers
Healthy male and/or female subjects.
Body Mass Index (BMI) of 17.5 to 30.5 kg/m2.
Total body weight >50 kg (110 lbs).
Use of prescription or nonprescription drugs and dietary supplements within 7 days or 5 half-lives (whichever is longer) prior to the first dose of study medication.
Use of tobacco- or nicotine-containing products in excess of the equivalent of 5 cigarettes per day.
Positive result for HIV-1, HIV-2, Hepatitis B serology (HbsAg, HbcAb) or anti hepatitis C virus serology (as determined by a multi antigen EIA).
All locations for NCT01597895
Pfizer Investigational Site
Bruxelles, Belgium, B-1070
View full eligibility
Tris trial is registered with FDA with number: NCT01597895. The sponsor of the trial is ViiV Healthcare and it is looking for 14 volunteers for the current phase.
Official trial title: Open-Label, Randomized, Fixed-Sequence, Crossover Study to Estimate the Effect of Telaprevir and Boceprevir on Maraviroc Pharmacokinetics in Healthy Subjects
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