TY - JOUR
T1 - Nelfinavir mesylate
AU - Tebas, Pablo
AU - Powderly, William G.
N1 - Funding Information:
Supported in part by K23AI01612, AI25903. This article is partially based in a previously published review [50]. We would like to thank Kristin Karpinsky for her help localising pertinent literature for the preparation of this manuscript.
PY - 2000
Y1 - 2000
N2 - Nelfinavir is an inhibitor of the HIV-1 and HIV-2 protease, with good in vivo activity in HIV-infected patients. Nelfinavir is used in combination with other antiretroviral medications as part of a potent antiretroviral regimen. When used in this manner, 50 - 75% of patients who are naïve to antiretro viral therapy have plasma HIV RNA levels below the limit of detection (< 400 copies) after 12 months of treatment. This use of nelfinavir in combina tion regimens is associated with an increase of almost 200/mm3 CD4+ lymphocytes at 12 months of therapy. Initial trials and clinical experience indicate that nelfinavir is equipotent to other potent protease inhibitors (Pis). The drug is well-tolerated, with mild diarrhoea being the most common side effect in 12 - 20% of patients. Virologie failure of nelfinavir is associated with genotypic and phenotypic changes that have a unique pattern that may retain susceptibility to other Pis. The results of small, non-controlled trials suggest these failures can be rescued with a second protease-based regimen. Due to the above characteristics, nelfinavir has become the most frequently prescribed first line PI.
AB - Nelfinavir is an inhibitor of the HIV-1 and HIV-2 protease, with good in vivo activity in HIV-infected patients. Nelfinavir is used in combination with other antiretroviral medications as part of a potent antiretroviral regimen. When used in this manner, 50 - 75% of patients who are naïve to antiretro viral therapy have plasma HIV RNA levels below the limit of detection (< 400 copies) after 12 months of treatment. This use of nelfinavir in combina tion regimens is associated with an increase of almost 200/mm3 CD4+ lymphocytes at 12 months of therapy. Initial trials and clinical experience indicate that nelfinavir is equipotent to other potent protease inhibitors (Pis). The drug is well-tolerated, with mild diarrhoea being the most common side effect in 12 - 20% of patients. Virologie failure of nelfinavir is associated with genotypic and phenotypic changes that have a unique pattern that may retain susceptibility to other Pis. The results of small, non-controlled trials suggest these failures can be rescued with a second protease-based regimen. Due to the above characteristics, nelfinavir has become the most frequently prescribed first line PI.
KW - Antiretroviral therapy
KW - HIV
KW - Nelfinavir
KW - Protease inhibitors
UR - http://www.scopus.com/inward/record.url?scp=0034568957&partnerID=8YFLogxK
U2 - 10.1517/14656566.1.7.1429
DO - 10.1517/14656566.1.7.1429
M3 - Article
C2 - 11249476
AN - SCOPUS:0034568957
SN - 1465-6566
VL - 1
SP - 1429
EP - 1440
JO - Expert Opinion on Pharmacotherapy
JF - Expert Opinion on Pharmacotherapy
IS - 7
ER -