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Single Dose IV Peramivir is Safe and Effective in the Treatment of Pediatric Influenza
BACKGROUND: Peramivir (PVR) is a potent neuraminidase inhibitor with in vitro activity against all influenza virus subtypes. Previous studies demonstrated the efficacy and safety of PVR as a single dose intravenous (IV) treatment for acute uncomplicated influenza in adults. METHODS: A phase 3 study...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5630974/ http://dx.doi.org/10.1093/ofid/ofx163.1861 |
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author | Vanchiere, John Plunkett, Stephanie Annamalai, Rajasekaran Julien, Katie Peterson, James Goisse, Marcy Christensen, Shane Mehta, Priyesh Coleman, Stephen Munoz, Flor Flynt, Amy Dobo, Sylvia Nagy, Eniko Kargl, Deborah Mathis, Amanda Collis, Phil Sheridan, William |
author_facet | Vanchiere, John Plunkett, Stephanie Annamalai, Rajasekaran Julien, Katie Peterson, James Goisse, Marcy Christensen, Shane Mehta, Priyesh Coleman, Stephen Munoz, Flor Flynt, Amy Dobo, Sylvia Nagy, Eniko Kargl, Deborah Mathis, Amanda Collis, Phil Sheridan, William |
author_sort | Vanchiere, John |
collection | PubMed |
description | BACKGROUND: Peramivir (PVR) is a potent neuraminidase inhibitor with in vitro activity against all influenza virus subtypes. Previous studies demonstrated the efficacy and safety of PVR as a single dose intravenous (IV) treatment for acute uncomplicated influenza in adults. METHODS: A phase 3 study compared age-appropriate doses of single dose IV PVR to 5 days of oral oseltamivir (OSE) (4:1 randomization, stratified by age) in pediatric subjects age 0 -17 years within 48 hours of onset of acute uncomplicated influenza. Plasma concentrations of PVR were measured up to 6 hours post dose. Serial viral titers were measured from nasopharyngeal swabs. Severity of influenza signs and symptoms were recorded in a diary. RESULTS: 122 subjects were enrolled up to a data cutoff of March 31, 2017 (<2 yrs, n = 7; 2-<7yrs, n = 37; 7-<13 yrs, n = 48; 13–17 yrs, n = 30). Interim results are reported for the first 108 subjects randomized, of which 101 (94%) received study drug. Influenza was confirmed by PCR in 75 (74%) subjects who received study drug (Intent-to-treat-Infected [ITTI] population). Key endpoints are summarized: CONCLUSION: Treatment of influenza in pediatric subjects with single dose IV PVR or 5 days of oral OSE was generally safe and well tolerated. Whilst not powered for efficacy differences, trends were observed in more rapid reduction in virus shedding and symptom alleviation for PVR treated subjects compared with OSE. The study continues to enroll subjects < 7 years. DISCLOSURES: J. Vanchiere, BioCryst Pharmaceuticals: Consultant and Investigator, Consulting fee and Research support; S. Plunkett, BioCryst Pharmaceuticals: Investigator, Research support; R. Annamalai, BioCryst Pharmaceuticals: Investigator, Research support; K. Julien, BioCryst Pharmaceuticals: Investigator, Research support; J. Peterson, BioCryst Pharmaceuticals: Investigator, Research support; M. Goisse, BioCryst Pharmaceuticals: Investigator, Research support; S. Christensen, BioCryst Pharmaceuticals: Investigator, Research support; P. Mehta, BioCryst Pharmaceuticals: Investigator, Research support; S. Coleman, BioCryst Pharmaceuticals: Investigator, Research support; F. Munoz, BioCryst Pharmaceuticals: Investigator, Research support; A. Flynt, BioCryst Pharmaceuticals: Consultant, Consulting fee; S. Dobo, BioCryst Pharmaceuticals: Employee, Salary; E. Nagy, BioCryst Pharmaceuticals: Employee, Salary; D. Kargl, BioCryst Pharmaceuticals: Consultant, Consulting fee; A. Mathis, BioCryst Pharmaceuticals: Employee, Salary; P. Collis, BioCryst Pharmaceuticals: Employee, Salary; W. Sheridan, BioCryst Pharmaceuticals: Employee, Salary |
format | Online Article Text |
id | pubmed-5630974 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-56309742017-11-07 Single Dose IV Peramivir is Safe and Effective in the Treatment of Pediatric Influenza Vanchiere, John Plunkett, Stephanie Annamalai, Rajasekaran Julien, Katie Peterson, James Goisse, Marcy Christensen, Shane Mehta, Priyesh Coleman, Stephen Munoz, Flor Flynt, Amy Dobo, Sylvia Nagy, Eniko Kargl, Deborah Mathis, Amanda Collis, Phil Sheridan, William Open Forum Infect Dis Abstracts BACKGROUND: Peramivir (PVR) is a potent neuraminidase inhibitor with in vitro activity against all influenza virus subtypes. Previous studies demonstrated the efficacy and safety of PVR as a single dose intravenous (IV) treatment for acute uncomplicated influenza in adults. METHODS: A phase 3 study compared age-appropriate doses of single dose IV PVR to 5 days of oral oseltamivir (OSE) (4:1 randomization, stratified by age) in pediatric subjects age 0 -17 years within 48 hours of onset of acute uncomplicated influenza. Plasma concentrations of PVR were measured up to 6 hours post dose. Serial viral titers were measured from nasopharyngeal swabs. Severity of influenza signs and symptoms were recorded in a diary. RESULTS: 122 subjects were enrolled up to a data cutoff of March 31, 2017 (<2 yrs, n = 7; 2-<7yrs, n = 37; 7-<13 yrs, n = 48; 13–17 yrs, n = 30). Interim results are reported for the first 108 subjects randomized, of which 101 (94%) received study drug. Influenza was confirmed by PCR in 75 (74%) subjects who received study drug (Intent-to-treat-Infected [ITTI] population). Key endpoints are summarized: CONCLUSION: Treatment of influenza in pediatric subjects with single dose IV PVR or 5 days of oral OSE was generally safe and well tolerated. Whilst not powered for efficacy differences, trends were observed in more rapid reduction in virus shedding and symptom alleviation for PVR treated subjects compared with OSE. The study continues to enroll subjects < 7 years. DISCLOSURES: J. Vanchiere, BioCryst Pharmaceuticals: Consultant and Investigator, Consulting fee and Research support; S. Plunkett, BioCryst Pharmaceuticals: Investigator, Research support; R. Annamalai, BioCryst Pharmaceuticals: Investigator, Research support; K. Julien, BioCryst Pharmaceuticals: Investigator, Research support; J. Peterson, BioCryst Pharmaceuticals: Investigator, Research support; M. Goisse, BioCryst Pharmaceuticals: Investigator, Research support; S. Christensen, BioCryst Pharmaceuticals: Investigator, Research support; P. Mehta, BioCryst Pharmaceuticals: Investigator, Research support; S. Coleman, BioCryst Pharmaceuticals: Investigator, Research support; F. Munoz, BioCryst Pharmaceuticals: Investigator, Research support; A. Flynt, BioCryst Pharmaceuticals: Consultant, Consulting fee; S. Dobo, BioCryst Pharmaceuticals: Employee, Salary; E. Nagy, BioCryst Pharmaceuticals: Employee, Salary; D. Kargl, BioCryst Pharmaceuticals: Consultant, Consulting fee; A. Mathis, BioCryst Pharmaceuticals: Employee, Salary; P. Collis, BioCryst Pharmaceuticals: Employee, Salary; W. Sheridan, BioCryst Pharmaceuticals: Employee, Salary Oxford University Press 2017-10-04 /pmc/articles/PMC5630974/ http://dx.doi.org/10.1093/ofid/ofx163.1861 Text en © The Author 2017. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Abstracts Vanchiere, John Plunkett, Stephanie Annamalai, Rajasekaran Julien, Katie Peterson, James Goisse, Marcy Christensen, Shane Mehta, Priyesh Coleman, Stephen Munoz, Flor Flynt, Amy Dobo, Sylvia Nagy, Eniko Kargl, Deborah Mathis, Amanda Collis, Phil Sheridan, William Single Dose IV Peramivir is Safe and Effective in the Treatment of Pediatric Influenza |
title | Single Dose IV Peramivir is Safe and Effective in the Treatment of Pediatric Influenza |
title_full | Single Dose IV Peramivir is Safe and Effective in the Treatment of Pediatric Influenza |
title_fullStr | Single Dose IV Peramivir is Safe and Effective in the Treatment of Pediatric Influenza |
title_full_unstemmed | Single Dose IV Peramivir is Safe and Effective in the Treatment of Pediatric Influenza |
title_short | Single Dose IV Peramivir is Safe and Effective in the Treatment of Pediatric Influenza |
title_sort | single dose iv peramivir is safe and effective in the treatment of pediatric influenza |
topic | Abstracts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5630974/ http://dx.doi.org/10.1093/ofid/ofx163.1861 |
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