Safety, Tolerability, and Antiretroviral Effects of Ritonavir-Nelfinavir Combination Therapy Administered for 48 Weeks
作者:
Charles Raines,
Charles Flexner,
Eugene Sun,
Margo Heath-Chiozzi,
Ronald Lewis,
Cathy Fields,
Carl Deetz,
Linda Apuzzo,
Susan Eshleman,
J. Jackson,
Joel Gallant,
期刊:
JAIDS Journal of Acquired Immune Deficiency Syndromes
(OVID Available online 2000)
卷期:
Volume 25,
issue 4
页码: 322-328
ISSN:1525-4135
年代: 2000
出版商: OVID
关键词: Antiretroviral therapy;Combination therapy;Protease inhibitors
数据来源: OVID
摘要:
ObjectiveTo evaluate the safety, tolerability, and anti-HIV activity of ritonavir-nelfinavir (RTV-NFV).DesignSingle-site, open-label, nonrandomized, multiple-dose trial of RTV combined with two doses of NFV in protease inhibitor (PI)-naive, HIV-infected patients.MethodsMean baseline HIV RNA was 39,500 copies/ml; mean baseline CD4 count was 323 cells/mm3. All patients received RTV at a dosage of 400 mg twice daily. Cohorts I (N= 10) and II (N= 10) received NFV at a dosage of 500 mg and 750 mg twice daily, respectively, for the initial 12 weeks of the study before allowing intensification with reverse transcriptase inhibitors.ResultsThe commonest effects of RTV-NFV therapy were study drug-related moderate-to-severe diarrhea (9 patients in cohorts I and II) and drug-related moderate-to-severe nausea (4 patients in cohorts I and II). HIV RNA was suppressed in a biphasic manner. At 48 weeks in cohort I, mean HIV RNA reduction was 2.82 log10copies/ml (standard error [SE] = .61;p= .001;N= 4); mean CD4 cell count increase was 236 cells/mm3(SE = 67.1;p= .006;N= 4). In cohort II, mean HIV RNA reduction at Week 48 was 2.21 log10copies/ml (SE = .430;p= .001;N= 8); mean CD4 cell count increase was 120 cells/mm3(SE = 47.5;p= .03;n= 8). In cohort I patients, 2 of 4 completing Week 48 had HIV RNA <20 copies/ml; and 3 of 4 had HIV RNA <400 copies/ml. In cohort II, 2 of 8 patients completing Week 48 had HIV RNA <20 copies/ml and 4 of 8 had HIV RNA <400 copies/ml. In addition, 3 patients in cohort I withdrew because of virologic failure not thought to be related to poor compliance. Moreover, 15 patients elected to add new reverse-transcriptase inhibitors (RTIs) after week 12.ConclusionsRTV-NFV with concomitant reverse transcriptase inhibitors is a potential dual-PI option for PI-naive patients.
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