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Pharmacokinetics and 48-week Safety and Antiviral Activity of Fosamprenavir-containing Regimens in HIV-infected 2- to 18-year-old Children
BACKGROUND: Pharmacokinetics, safety and antiviral activity of twice-daily fosamprenavir with or without ritonavir were evaluated in 2- to 18-year-old protease inhibitor–naïve and -experienced HIV-1–infected children. METHODS: Serial pharmacokinetic samples were collected at week 2 and predose sampl...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Williams & Wilkins
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3882305/ https://www.ncbi.nlm.nih.gov/pubmed/23811744 http://dx.doi.org/10.1097/INF.0b013e3182a1126a |
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author | Fortuny, Claudia Duiculescu, Dan Cheng, Katharine Garges, Harmony P. Cotton, Mark Tamarirt, Desamparados Pérez Ford, Susan L. Wire, Mary Beth Givens, Naomi Ross, Lisa L. Lou, Yu Perger, Teodora Sievers, Jörg |
author_facet | Fortuny, Claudia Duiculescu, Dan Cheng, Katharine Garges, Harmony P. Cotton, Mark Tamarirt, Desamparados Pérez Ford, Susan L. Wire, Mary Beth Givens, Naomi Ross, Lisa L. Lou, Yu Perger, Teodora Sievers, Jörg |
author_sort | Fortuny, Claudia |
collection | PubMed |
description | BACKGROUND: Pharmacokinetics, safety and antiviral activity of twice-daily fosamprenavir with or without ritonavir were evaluated in 2- to 18-year-old protease inhibitor–naïve and -experienced HIV-1–infected children. METHODS: Serial pharmacokinetic samples were collected at week 2 and predose samples every 4–12 weeks. Safety and plasma HIV-1 RNA were monitored every 4–12 weeks. RESULTS: Twenty protease inhibitor–naïve 2- to <6-year-old subjects received antiretroviral treatment including unboosted fosamprenavir twice-daily, whereas 89 protease inhibitor–naïve and -experienced 2- to 18-year-old subjects received fosamprenavir/ritonavir-containing therapy twice-daily. Median fosamprenavir exposure was 891 days (range 15–1805 days), with 88% exposed >48 weeks. Twice-daily doses of fosamprenavir/ritonavir 23/3 mg/kg in 2- to <6-year olds, 18/3 mg/kg in ≥6-year olds and 700/100 mg in adolescents achieved plasma amprenavir exposures comparable with or higher than 700/100 mg twice-daily in adults while fosamprenavir 30 mg/kg twice-daily in 2- to <6-year olds led to exposures higher than 1400 mg twice-daily in adults. The proportion of subjects with HIV-1 RNA <400 copies/mL at week 48 was 60% for fosamprenavir and 53–74% for fosamprenavir/ritonavir (intent-to-treat [exposed], snapshot analysis). Median increases in absolute and relative (percentage) CD4 counts from baseline to week 48 occurred in both the fosamprenavir (340 cells/mm(3); 8%) and fosamprenavir/ritonavir group (190 cells/mm(3); 8%). The most common adverse events were vomiting, cough, and diarrhea; 18 subjects experienced serious adverse events, including 9 with suspected abacavir hypersensitivity. CONCLUSIONS: Fosamprenavir regimens administered to HIV-1–infected children aged 2–18 years were generally well-tolerated and provided sustained antiviral activity over 48 weeks, with plasma amprenavir exposures comparable with or higher than adults. |
format | Online Article Text |
id | pubmed-3882305 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-38823052014-01-07 Pharmacokinetics and 48-week Safety and Antiviral Activity of Fosamprenavir-containing Regimens in HIV-infected 2- to 18-year-old Children Fortuny, Claudia Duiculescu, Dan Cheng, Katharine Garges, Harmony P. Cotton, Mark Tamarirt, Desamparados Pérez Ford, Susan L. Wire, Mary Beth Givens, Naomi Ross, Lisa L. Lou, Yu Perger, Teodora Sievers, Jörg Pediatr Infect Dis J HIV Reports BACKGROUND: Pharmacokinetics, safety and antiviral activity of twice-daily fosamprenavir with or without ritonavir were evaluated in 2- to 18-year-old protease inhibitor–naïve and -experienced HIV-1–infected children. METHODS: Serial pharmacokinetic samples were collected at week 2 and predose samples every 4–12 weeks. Safety and plasma HIV-1 RNA were monitored every 4–12 weeks. RESULTS: Twenty protease inhibitor–naïve 2- to <6-year-old subjects received antiretroviral treatment including unboosted fosamprenavir twice-daily, whereas 89 protease inhibitor–naïve and -experienced 2- to 18-year-old subjects received fosamprenavir/ritonavir-containing therapy twice-daily. Median fosamprenavir exposure was 891 days (range 15–1805 days), with 88% exposed >48 weeks. Twice-daily doses of fosamprenavir/ritonavir 23/3 mg/kg in 2- to <6-year olds, 18/3 mg/kg in ≥6-year olds and 700/100 mg in adolescents achieved plasma amprenavir exposures comparable with or higher than 700/100 mg twice-daily in adults while fosamprenavir 30 mg/kg twice-daily in 2- to <6-year olds led to exposures higher than 1400 mg twice-daily in adults. The proportion of subjects with HIV-1 RNA <400 copies/mL at week 48 was 60% for fosamprenavir and 53–74% for fosamprenavir/ritonavir (intent-to-treat [exposed], snapshot analysis). Median increases in absolute and relative (percentage) CD4 counts from baseline to week 48 occurred in both the fosamprenavir (340 cells/mm(3); 8%) and fosamprenavir/ritonavir group (190 cells/mm(3); 8%). The most common adverse events were vomiting, cough, and diarrhea; 18 subjects experienced serious adverse events, including 9 with suspected abacavir hypersensitivity. CONCLUSIONS: Fosamprenavir regimens administered to HIV-1–infected children aged 2–18 years were generally well-tolerated and provided sustained antiviral activity over 48 weeks, with plasma amprenavir exposures comparable with or higher than adults. Williams & Wilkins 2014-01 2013-12-12 /pmc/articles/PMC3882305/ /pubmed/23811744 http://dx.doi.org/10.1097/INF.0b013e3182a1126a Text en Copyright © 2014 by Lippincott Williams & Wilkins http://creativecommons.org/licenses/by-nc-nd/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivitives 3.0 License, where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially. |
spellingShingle | HIV Reports Fortuny, Claudia Duiculescu, Dan Cheng, Katharine Garges, Harmony P. Cotton, Mark Tamarirt, Desamparados Pérez Ford, Susan L. Wire, Mary Beth Givens, Naomi Ross, Lisa L. Lou, Yu Perger, Teodora Sievers, Jörg Pharmacokinetics and 48-week Safety and Antiviral Activity of Fosamprenavir-containing Regimens in HIV-infected 2- to 18-year-old Children |
title | Pharmacokinetics and 48-week Safety and Antiviral Activity of Fosamprenavir-containing Regimens in HIV-infected 2- to 18-year-old Children |
title_full | Pharmacokinetics and 48-week Safety and Antiviral Activity of Fosamprenavir-containing Regimens in HIV-infected 2- to 18-year-old Children |
title_fullStr | Pharmacokinetics and 48-week Safety and Antiviral Activity of Fosamprenavir-containing Regimens in HIV-infected 2- to 18-year-old Children |
title_full_unstemmed | Pharmacokinetics and 48-week Safety and Antiviral Activity of Fosamprenavir-containing Regimens in HIV-infected 2- to 18-year-old Children |
title_short | Pharmacokinetics and 48-week Safety and Antiviral Activity of Fosamprenavir-containing Regimens in HIV-infected 2- to 18-year-old Children |
title_sort | pharmacokinetics and 48-week safety and antiviral activity of fosamprenavir-containing regimens in hiv-infected 2- to 18-year-old children |
topic | HIV Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3882305/ https://www.ncbi.nlm.nih.gov/pubmed/23811744 http://dx.doi.org/10.1097/INF.0b013e3182a1126a |
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