Due to its long half-life (25-30 hours) the once daily administration of ne
virapine would appear logical but we do not have data regarding the tolerab
ility and efficacy of this schedule. We have therefore tried to evaluate th
is schedule in 93 HIV-infected patients beginning a treatment containing ne
virapine. The tolerability of once daily nevirapine was similar to the usua
l schedule with 15% of mucocutaneous allergy. The immunologic and virologic
efficacy of once daily nevirapine was confirmed with a mean RNA HIV decrea
se of 1.4 log, 1.3 log, 1.1 log and 1.3 log at M1, M3, M6 and M9 respective
ly. The best results were observed in naive patients. Residual plasma conce
ntration of nevirapine was performed in 35 patients with a mean value of 3,
8 mg/l.