Amprenavir is the fifth protease inhibitor approved by the FDA. Studies eva
luating surrogate endpoints have determined that adding amprenavir to a dua
l nucleoside reverse transcriptase regimen significantly reduces Viral load
after 16 weeks of therapy. in these studies, amprenavir was more effective
in antiretroviral-naive subjects than in those previously exposed to antir
etroviral therapy, Adverse effects associated with amprenavir include gastr
ointestinal complaints, rash, and paresthesias, A phase II study in pediatr
ic patients found safety and efficacy results similar to those in adults. L
ike other members of this drug class, amprenavir inhibits the cytochrome P4
50 3A4 enzyme, resulting in multiple drug interactions. Because of amprenav
ir's relatively long half-life allowing twice-daily dosing, amprenavir-cont
aining regimens have the potential to improve adherence and, potentially to
reduce the emergence of resistance.