HIV Infections Clinical Trial
Official title:
Plasma and Intracellular Concentrations of Raltegravir and Etravirine Administered Once Daily (800 mg and 400 mg, Respectively) Compared With Standard Dosing (400 mg and 200 mg/12 h) in Patients With HIV Infection
Hypothesis: the intracellular concentrations of raltegravir (RAL) and etravirine (ETV)
administrated as 800 and 400 mg once a day, respectively, are similar to those obtained with
the standard doses of 400 and 200 mg/12h, respectively.
Objective: To analyze the plasma and intracellular concentrations of RAL and ETV
administrated as 800 and 400 mg once daily respectively compared with standard doses of 400
and 200 mg/12h, respectively, and if they support its once daily administration.
Objective: To analyze the plasma and intracellular concentrations of RAL and ETV
administrated as 800 and 400 mg once daily respectively compared with standard doses of 400
and 200 mg/12h, respectively, and if they support its once daily administration.
Method: Phase IV, prospective, open labelled clinical trial with a planned duration of 24
weeks in which 16 patients from Hospitales Universitarios Virgen del Rocío will be enrolled.
A 12 hours pharmacokinetic profile (immediately before and after 1, 2, 3, 4, 6, 8, 10 and 12
h) will be obtained after a supervised drug intake while taking RAL or ETV bid.
Afterwards,the patients will take RAL or ETV once a day for 7 - 10 days. Subsequently, a new
pharmacokinetic profile (predose and after 1, 2, 3, 4, 6, 8, 10, 12, 16, 20 and 24 h after a
supervised drug intake) will be obtained.
;
Allocation: Non-Randomized, Endpoint Classification: Pharmacokinetics Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Treatment
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