Cargando…
Standardising neonatal and paediatric antibiotic clinical trial design and conduct: the PENTA-ID network view
Antimicrobial development for children remains challenging due to multiple barriers to conducting randomised clinical trials (CTs). There is currently considerable heterogeneity in the design and conduct of paediatric antibiotic studies, hampering comparison and meta-analytic approaches. The board o...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6955510/ https://www.ncbi.nlm.nih.gov/pubmed/31892658 http://dx.doi.org/10.1136/bmjopen-2019-032592 |
_version_ | 1783486945212497920 |
---|---|
author | Folgori, Laura Lutsar, Irja Standing, Joseph F Walker, A Sarah Roilides, Emmanuel Zaoutis, Theoklis E Jafri, Hasan Giaquinto, Carlo Turner, Mark A Sharland, Mike |
author_facet | Folgori, Laura Lutsar, Irja Standing, Joseph F Walker, A Sarah Roilides, Emmanuel Zaoutis, Theoklis E Jafri, Hasan Giaquinto, Carlo Turner, Mark A Sharland, Mike |
author_sort | Folgori, Laura |
collection | PubMed |
description | Antimicrobial development for children remains challenging due to multiple barriers to conducting randomised clinical trials (CTs). There is currently considerable heterogeneity in the design and conduct of paediatric antibiotic studies, hampering comparison and meta-analytic approaches. The board of the European networks for paediatric research at the European Medicines Agency (EMA), in collaboration with the Paediatric European Network for Treatments of AIDS—Infectious Diseases network (www.penta-id.org), recently developed a Working Group on paediatric antibiotic CT design, involving academic, regulatory and industry representatives. The evidence base for any specific criteria for the design and conduct of efficacy and safety antibiotic trials for children is very limited and will evolve over time as further studies are conducted. The suggestions being put forward here are based on the adult EMA guidance, adapted for neonates and children. In particular, this document provides suggested guidance on the general principles of harmonisation between regulatory and strategic trials, including (1) standardised key inclusion/exclusion criteria and widely applicable outcome measures for specific clinical infectious syndromes (CIS) to be used in CTs on efficacy of antibiotic in children; (2) key components of safety that should be reported in paediatric antibiotic CTs; (3) standardised sample sizes for safety studies. Summarising views from a range of key stakeholders, specific criteria for the design and conduct of efficacy and safety antibiotic trials in specific CIS for children have been suggested. The recommended criteria are intended to be applicable to both regulatory and clinical investigator-led strategic trials and could be the basis for harmonisation in the design and conduct of CTs on antibiotics in children. The next step is further discussion internationally with investigators, paediatric CTs networks and regulators. |
format | Online Article Text |
id | pubmed-6955510 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-69555102020-01-27 Standardising neonatal and paediatric antibiotic clinical trial design and conduct: the PENTA-ID network view Folgori, Laura Lutsar, Irja Standing, Joseph F Walker, A Sarah Roilides, Emmanuel Zaoutis, Theoklis E Jafri, Hasan Giaquinto, Carlo Turner, Mark A Sharland, Mike BMJ Open Paediatrics Antimicrobial development for children remains challenging due to multiple barriers to conducting randomised clinical trials (CTs). There is currently considerable heterogeneity in the design and conduct of paediatric antibiotic studies, hampering comparison and meta-analytic approaches. The board of the European networks for paediatric research at the European Medicines Agency (EMA), in collaboration with the Paediatric European Network for Treatments of AIDS—Infectious Diseases network (www.penta-id.org), recently developed a Working Group on paediatric antibiotic CT design, involving academic, regulatory and industry representatives. The evidence base for any specific criteria for the design and conduct of efficacy and safety antibiotic trials for children is very limited and will evolve over time as further studies are conducted. The suggestions being put forward here are based on the adult EMA guidance, adapted for neonates and children. In particular, this document provides suggested guidance on the general principles of harmonisation between regulatory and strategic trials, including (1) standardised key inclusion/exclusion criteria and widely applicable outcome measures for specific clinical infectious syndromes (CIS) to be used in CTs on efficacy of antibiotic in children; (2) key components of safety that should be reported in paediatric antibiotic CTs; (3) standardised sample sizes for safety studies. Summarising views from a range of key stakeholders, specific criteria for the design and conduct of efficacy and safety antibiotic trials in specific CIS for children have been suggested. The recommended criteria are intended to be applicable to both regulatory and clinical investigator-led strategic trials and could be the basis for harmonisation in the design and conduct of CTs on antibiotics in children. The next step is further discussion internationally with investigators, paediatric CTs networks and regulators. BMJ Publishing Group 2019-12-31 /pmc/articles/PMC6955510/ /pubmed/31892658 http://dx.doi.org/10.1136/bmjopen-2019-032592 Text en © Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Paediatrics Folgori, Laura Lutsar, Irja Standing, Joseph F Walker, A Sarah Roilides, Emmanuel Zaoutis, Theoklis E Jafri, Hasan Giaquinto, Carlo Turner, Mark A Sharland, Mike Standardising neonatal and paediatric antibiotic clinical trial design and conduct: the PENTA-ID network view |
title | Standardising neonatal and paediatric antibiotic clinical trial design and conduct: the PENTA-ID network view |
title_full | Standardising neonatal and paediatric antibiotic clinical trial design and conduct: the PENTA-ID network view |
title_fullStr | Standardising neonatal and paediatric antibiotic clinical trial design and conduct: the PENTA-ID network view |
title_full_unstemmed | Standardising neonatal and paediatric antibiotic clinical trial design and conduct: the PENTA-ID network view |
title_short | Standardising neonatal and paediatric antibiotic clinical trial design and conduct: the PENTA-ID network view |
title_sort | standardising neonatal and paediatric antibiotic clinical trial design and conduct: the penta-id network view |
topic | Paediatrics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6955510/ https://www.ncbi.nlm.nih.gov/pubmed/31892658 http://dx.doi.org/10.1136/bmjopen-2019-032592 |
work_keys_str_mv | AT folgorilaura standardisingneonatalandpaediatricantibioticclinicaltrialdesignandconductthepentaidnetworkview AT lutsarirja standardisingneonatalandpaediatricantibioticclinicaltrialdesignandconductthepentaidnetworkview AT standingjosephf standardisingneonatalandpaediatricantibioticclinicaltrialdesignandconductthepentaidnetworkview AT walkerasarah standardisingneonatalandpaediatricantibioticclinicaltrialdesignandconductthepentaidnetworkview AT roilidesemmanuel standardisingneonatalandpaediatricantibioticclinicaltrialdesignandconductthepentaidnetworkview AT zaoutistheoklise standardisingneonatalandpaediatricantibioticclinicaltrialdesignandconductthepentaidnetworkview AT jafrihasan standardisingneonatalandpaediatricantibioticclinicaltrialdesignandconductthepentaidnetworkview AT giaquintocarlo standardisingneonatalandpaediatricantibioticclinicaltrialdesignandconductthepentaidnetworkview AT turnermarka standardisingneonatalandpaediatricantibioticclinicaltrialdesignandconductthepentaidnetworkview AT sharlandmike standardisingneonatalandpaediatricantibioticclinicaltrialdesignandconductthepentaidnetworkview |