HIV-1-infection Clinical Trial
Official title:
Virological Efficacy and Safety of Etravirine Plus 2 Active Nucleos(t)Ide Reverse-transcriptase Inhibitors (NRTIs) in HIV-1-infected Patients
The purpose of this study is to evaluate the virological and clinical efficacy of etravirine plus 2 active nucleos(t)ide reverse-transcriptase inhibitors (NRTIs) in HIV-infected patients. Additionally, the safety of these regimens, specially lipid profiles, will be assessed.
Methods: prospective, single arm multicenter clinical trial without entry restrictions on
plasma HIV-RNA (VL) or CD4 with a planned duration of 52 weeks.
The primary clinical endpoint is the percentage of subjects with therapeutic success on
etravirine 400 mg/day (200 mg bid or 400 mg qd) plus 2 active NRTIs after 12 months.
Efficacy data will be analyzed by on-treatment and by intention-to-treat analyses
(noncomplete/missing equals failure), considering treatment failure as either treatment
interruption whatever the reason (adverse events, death, or loss to follow-up) or
virological failure, defined as inability to suppress the VL to less than 50 copies/ml after
24 weeks on treatment or a confirmed VL of more than 200 copies/ml in patients who had
previously achieved a viral suppression or had an undetectable viral load at inclusion.
Patients missing two consecutive scheduled visits were considered lost to follow-up. The
safety and tolerability of the studied medications will be evaluated by means of clinical
adverse events, physical examination and laboratory results.
NRTIs prescribed as part of HAART were selected by the responsible physicians on the basis
of previous antiretroviral treatments and/or genotypic resistance testing.
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Observational Model: Cohort, Time Perspective: Prospective
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