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Novel study design to assess the efficacy and tolerability of antiseizure medications for focal‐onset seizures in infants and young children: A consensus document from the regulatory task force and the pediatric commission of the International League against Epilepsy (ILAE), in collaboration with the Pediatric Epilepsy Research Consortium (PERC)
High‐quality placebo‐controlled drug trials for focal‐onset seizures in infants and children younger than 4 years have become increasingly difficult to perform because of eligibility constraints and onerous study designs. Traditional designs used in these populations require a high baseline seizure...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6885693/ https://www.ncbi.nlm.nih.gov/pubmed/31819909 http://dx.doi.org/10.1002/epi4.12356 |
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author | Auvin, Stéphane French, Jacqueline Dlugos, Denis Knupp, Kelly G. Perucca, Emilio Arzimanoglou, Alexis Whalen, Ed Shellhaas, Renée A. |
author_facet | Auvin, Stéphane French, Jacqueline Dlugos, Denis Knupp, Kelly G. Perucca, Emilio Arzimanoglou, Alexis Whalen, Ed Shellhaas, Renée A. |
author_sort | Auvin, Stéphane |
collection | PubMed |
description | High‐quality placebo‐controlled drug trials for focal‐onset seizures in infants and children younger than 4 years have become increasingly difficult to perform because of eligibility constraints and onerous study designs. Traditional designs used in these populations require a high baseline seizure frequency, two hospitalizations for video‐electroencephalography (video‐EEG) monitoring, and willingness to accept potential exposure to placebo when the drugs to be tested are usually already available for off‐label prescription. To address these constraints, the International League Against Epilepsy (ILAE) regulatory taskforce and the ILAE pediatric commission, in collaboration with the Pediatric Epilepsy Research Consortium (PERC), propose a novel trial design which involves seizure counting by caregivers based on previous video‐EEG/video validation of specific seizure semiologies. We present a novel randomized placebo‐controlled trial design intended to be used for studying new antiseizure medications (ASMs) for focal‐onset seizures (FOS) in children aged one month to four years. This design uses “time to Nth seizure” as the primary outcome and incorporates a new element of variable baseline duration. This approach permits enrollment of infants with lower seizure burden, who might not have video‐EEG‐recorded seizures within 2‐3 days of monitoring. Repeated hospitalizations for video‐EEG recordings are avoided, and duration of baseline and exposure to placebo or ineffective treatment(s) are minimized. By broadening eligibility criteria, reducing risks from prolonged placebo exposure, and relying on validated recording of seizure counting by caregivers, clinical trials will be likely to be completed more efficiently than in the recent past. |
format | Online Article Text |
id | pubmed-6885693 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-68856932019-12-09 Novel study design to assess the efficacy and tolerability of antiseizure medications for focal‐onset seizures in infants and young children: A consensus document from the regulatory task force and the pediatric commission of the International League against Epilepsy (ILAE), in collaboration with the Pediatric Epilepsy Research Consortium (PERC) Auvin, Stéphane French, Jacqueline Dlugos, Denis Knupp, Kelly G. Perucca, Emilio Arzimanoglou, Alexis Whalen, Ed Shellhaas, Renée A. Epilepsia Open Special Reports High‐quality placebo‐controlled drug trials for focal‐onset seizures in infants and children younger than 4 years have become increasingly difficult to perform because of eligibility constraints and onerous study designs. Traditional designs used in these populations require a high baseline seizure frequency, two hospitalizations for video‐electroencephalography (video‐EEG) monitoring, and willingness to accept potential exposure to placebo when the drugs to be tested are usually already available for off‐label prescription. To address these constraints, the International League Against Epilepsy (ILAE) regulatory taskforce and the ILAE pediatric commission, in collaboration with the Pediatric Epilepsy Research Consortium (PERC), propose a novel trial design which involves seizure counting by caregivers based on previous video‐EEG/video validation of specific seizure semiologies. We present a novel randomized placebo‐controlled trial design intended to be used for studying new antiseizure medications (ASMs) for focal‐onset seizures (FOS) in children aged one month to four years. This design uses “time to Nth seizure” as the primary outcome and incorporates a new element of variable baseline duration. This approach permits enrollment of infants with lower seizure burden, who might not have video‐EEG‐recorded seizures within 2‐3 days of monitoring. Repeated hospitalizations for video‐EEG recordings are avoided, and duration of baseline and exposure to placebo or ineffective treatment(s) are minimized. By broadening eligibility criteria, reducing risks from prolonged placebo exposure, and relying on validated recording of seizure counting by caregivers, clinical trials will be likely to be completed more efficiently than in the recent past. John Wiley and Sons Inc. 2019-09-04 /pmc/articles/PMC6885693/ /pubmed/31819909 http://dx.doi.org/10.1002/epi4.12356 Text en © 2019 The Authors. Epilepsia Open published by Wiley Periodicals Inc. on behalf of International League Against Epilepsy. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Special Reports Auvin, Stéphane French, Jacqueline Dlugos, Denis Knupp, Kelly G. Perucca, Emilio Arzimanoglou, Alexis Whalen, Ed Shellhaas, Renée A. Novel study design to assess the efficacy and tolerability of antiseizure medications for focal‐onset seizures in infants and young children: A consensus document from the regulatory task force and the pediatric commission of the International League against Epilepsy (ILAE), in collaboration with the Pediatric Epilepsy Research Consortium (PERC) |
title | Novel study design to assess the efficacy and tolerability of antiseizure medications for focal‐onset seizures in infants and young children: A consensus document from the regulatory task force and the pediatric commission of the International League against Epilepsy (ILAE), in collaboration with the Pediatric Epilepsy Research Consortium (PERC) |
title_full | Novel study design to assess the efficacy and tolerability of antiseizure medications for focal‐onset seizures in infants and young children: A consensus document from the regulatory task force and the pediatric commission of the International League against Epilepsy (ILAE), in collaboration with the Pediatric Epilepsy Research Consortium (PERC) |
title_fullStr | Novel study design to assess the efficacy and tolerability of antiseizure medications for focal‐onset seizures in infants and young children: A consensus document from the regulatory task force and the pediatric commission of the International League against Epilepsy (ILAE), in collaboration with the Pediatric Epilepsy Research Consortium (PERC) |
title_full_unstemmed | Novel study design to assess the efficacy and tolerability of antiseizure medications for focal‐onset seizures in infants and young children: A consensus document from the regulatory task force and the pediatric commission of the International League against Epilepsy (ILAE), in collaboration with the Pediatric Epilepsy Research Consortium (PERC) |
title_short | Novel study design to assess the efficacy and tolerability of antiseizure medications for focal‐onset seizures in infants and young children: A consensus document from the regulatory task force and the pediatric commission of the International League against Epilepsy (ILAE), in collaboration with the Pediatric Epilepsy Research Consortium (PERC) |
title_sort | novel study design to assess the efficacy and tolerability of antiseizure medications for focal‐onset seizures in infants and young children: a consensus document from the regulatory task force and the pediatric commission of the international league against epilepsy (ilae), in collaboration with the pediatric epilepsy research consortium (perc) |
topic | Special Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6885693/ https://www.ncbi.nlm.nih.gov/pubmed/31819909 http://dx.doi.org/10.1002/epi4.12356 |
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