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You can access this
if you have
and you are
between 18 and 55
This is an early phase trial to determine
the dosage and safety of the new treatment.
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The purpose of this study is to determine the effect that telaprevir and boceprevir has on the pharmacokinetics of maraviroc.
Maraviroc + Boceprevir
Maraviroc + Telaprevir
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Locations near you
Unfortunately, there are no recruiting locations near you. Please check the list with all locations below.
Full eligibility criteria for NCT01597895
Ages eligible for Study
18 Years to 55 Years
Genders eligible for Study
Accepts Healthy Volunteers
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:
. The sponsor of the trial is
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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My condition is
I am a healthy volunteer
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