Literature DB >> 15259905

Pharmacokinetics of once-daily saquinavir/ritonavir in HIV-infected subjects: comparison with the standard twice-daily regimen.

Marta Boffito1, Laura Dickinson, Andrew Hill, David Back, Graeme Moyle, Mark Nelson, Chris Higgs, Carl Fletcher, Sundhiya Mandalia, Brian Gazzard, Anton Pozniak.   

Abstract

OBJECTIVE: To evaluate the steady-state pharmacokinetics and safety of two once-daily saquinavir/ritonavir (SQV/RTV) regimens, 1600/100 and 2000/100 mg, in HIV-positive patients.
METHODS: Eighteen HIV-infected adults treated with the standard twice-daily SQV/RTV 1000/100 mg regimen were enrolled in this open-label, two-phase, crossover pharmacokinetic study. The steady-state pharmacokinetics of SQV administered with 100 mg RTV were investigated following once-daily doses of 1600 mg or 2000 mg or a twice-daily dose of 1000 mg. Plasma drug concentrations were determined by high performance liquid chromatography-tandem mass spectrometry and pharmacokinetic parameters were calculated using a non-compartmental model.
RESULTS: Compared with SQV 1000 mg twice daily, the Cmax of SQV following a 1600 mg and 2000 mg dose increased in a dose-proportional manner [geometric mean (95% CI) 1915 (1656-2850) ng/ml for 1000 mg, 2782 (2249-4330) ng/ml for 1600 mg and 4179 (3429-6105) ng/ml for 2000 mg doses, respectively]. SQV Ctrough values were 539 (453-1011), 106 (76-223) and 231 (75-822) ng/ml, respectively. A SQV Ctrough value greater than 100 ng/ml was achieved in all subjects on the twice-daily regimen, in 9/18 (50%) subjects on the 1600/100 mg once-daily regimen, and in 14/17 (82%) subjects on the 2000/100 mg once-daily regimen. The once-daily regimens were well tolerated, with mild-to-moderate gastrointestinal symptoms being the only events reported by a small number of patients.
CONCLUSION: This is the first study to evaluate the pharmacokinetics of once-daily SQV/RTV 2000/100 mg in HIV-infected subjects. Our findings suggest that this regimen may be an alternative to twice-daily 1000/100 mg doses and should be further evaluated in efficacy studies. The data indicate that most patients (14/17) on once-daily 2000/100 mg achieve trough concentrations above target values (determined for HIV wild-type) for efficacy of SQV with the use of just 100 mg RTV/day and with good tolerability.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 15259905

Source DB:  PubMed          Journal:  Antivir Ther        ISSN: 1359-6535


  5 in total

1.  Clinical and pharmacokinetic data support once-daily low-dose boosted saquinavir (1,200 milligrams saquinavir with 100 milligrams ritonavir) in treatment-naive or limited protease inhibitor-experienced human immunodeficiency virus-infected patients.

Authors:  Ana Marin-Niebla; Luis Fernando Lopez-Cortes; Rosa Ruiz-Valderas; Pompeyo Viciana; Rosario Mata; Alicia Gutierrez; Rosario Pascual; Magdalena Rodriguez
Journal:  Antimicrob Agents Chemother       Date:  2007-03-19       Impact factor: 5.191

2.  Population pharmacokinetics of ritonavir-boosted saquinavir regimens in HIV-infected individuals.

Authors:  Laura Dickinson; Marta Boffito; David J Back; Saye H Khoo; Anton L Pozniak; Peter Mugyenyi; Concepta Merry; Reshma Saskia Autar; David M Burger; Leon J Aarons
Journal:  J Antimicrob Chemother       Date:  2008-09-29       Impact factor: 5.790

3.  Efficacy, safety and pharmacokinetic of once-daily boosted saquinavir (1500/100 mg) together with 2 nucleos(t)ide reverse transcriptase inhibitors in real life: a multicentre prospective study.

Authors:  Luis F López-Cortés; Pompeyo Viciana; Rosa Ruiz-Valderas; Juan Pasquau; Josefa Ruiz; Fernando Lozano; Dolores Merino; Antonio Vergara; Alberto Terrón; Luis González; Antonio Rivero; Agustin Muñoz-Sanz
Journal:  AIDS Res Ther       Date:  2010-03-17       Impact factor: 2.250

4.  Pharmacokinetic analysis to assess forgiveness of boosted saquinavir regimens for missed or late dosing.

Authors:  Laura Dickinson; Marta Boffito; Saye H Khoo; Malte Schutz; Leon J Aarons; Anton L Pozniak; David J Back
Journal:  J Antimicrob Chemother       Date:  2008-05-07       Impact factor: 5.790

5.  Effect of a modified saquinavir/ritonavir dosing regimen with lower dose lead-in phase on QTc interval, pharmacokinetics, antiviral activity and safety in treatment-naïve HIV-1-infected patients.

Authors:  Marta Boffito; Akil Jackson; Anton Pozniak; Mylene Giraudon; Rohit Kulkarni; Maria Connie Abelardo; Indravadan H Patel; Peter N Morcos
Journal:  Drugs R D       Date:  2015-03
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.