Addressing the barriers to pediatric drug development

workshop summary

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Last edited by ImportBot
March 19, 2023 | History

Addressing the barriers to pediatric drug development

workshop summary

Decades of research have demonstrated that children do not respond to medications in the same way as adults. Differences between children and adults in the overall response to medications are due to profound anatomical, physiological, and developmental differences. Although few would argue that children should receive medications that have not been adequately tested for safety and efficacy, the majority of drugs prescribed for children--50 to 75 percent-- have not been tested in pediatric populations. Without adequate data from such testing, prescribing drugs appropriately becomes challenging for clinicians treating children, from infancy through adolescence. Addressing the Barriers to Pediatric Drug Development is the summary of a workshop, held in Washington, D.C. on June 13, 2006, that was organized to identify barriers to the development and testing of drugs for pediatric populations, as well as ways in which the system can be improved to facilitate better treatments for children.

Publish Date
Language
English
Pages
52

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Edition Availability
Cover of: Addressing the Barriers to Pediatric Drug Development
Addressing the Barriers to Pediatric Drug Development: Workshop Summary
2009, National Academies Press
in English
Cover of: Addressing the barriers to pediatric drug development
Addressing the barriers to pediatric drug development: workshop summary
2008, National Academies Press
in English
Cover of: Addressing the barriers to pediatric drug development
Addressing the barriers to pediatric drug development: workshop summary
2008, National Academies Press
in English

Add another edition?

Book Details


Table of Contents

Introduction
Response to drugs in various age groups
Product labeling
Organization of this summary
Regulatory framework
Best pharmaceuticals for children act
Pediatric Research Equity Act
Impact of pediatric drug legislation
Discussion
Current challenges in developing and prescribing drugs for children
Barriers to pediatric drug development
Formulations
Dosing, bioavailability, and drug response
Models for enhancing pediatric drug development
Vaccine development in the United States
The European Union's new regulatory approach
The St. Jude's model for pediatric oncology drugs
Challenges and opportunities for the future
Systemic solutions
Elimination of economic barriers
Concluding thoughts.

Edition Notes

Includes bibliographical references (p. 41-42).

Also available on the World Wide Web.

Published in
Washington, D.C
Genre
Congresses

Classifications

Library of Congress
RJ560 .A33 2008,

The Physical Object

Pagination
xii, 52 p. ;
Number of pages
52

ID Numbers

Open Library
OL23607007M
ISBN 10
0309107423
ISBN 13
9780309107426
LCCN
2009285666
Goodreads
5794973

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History

Download catalog record: RDF / JSON
March 19, 2023 Edited by ImportBot import existing book
August 1, 2020 Edited by ImportBot import existing book
February 11, 2019 Created by MARC Bot import existing book