Literature DB >> 25963725

Failed Pediatric Drug Development Trials.

J D Momper1, Y Mulugeta2, G J Burckart2.   

Abstract

Pediatric product development initiatives have stimulated the development of therapies for children, resulting in improved product labeling, increased identification of adverse events, and development of new pediatric formulations. However, 42% of recently completed pediatric trials have failed to establish either safety or efficacy, leading to an inability to label the product for use in children.(1) Characterizing these failed trials, including common contributing factors, is imperative to designing better pediatric trials in the future.
© 2015 American Society for Clinical Pharmacology and Therapeutics.

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Year:  2015        PMID: 25963725     DOI: 10.1002/cpt.142

Source DB:  PubMed          Journal:  Clin Pharmacol Ther        ISSN: 0009-9236            Impact factor:   6.875


  23 in total

Review 1.  Development of Drug Therapies for Newborns and Children: The Scientific and Regulatory Imperatives.

Authors:  Yeruk Lily Mulugeta; Anne Zajicek; Jeff Barrett; Hari Cheryl Sachs; Susan McCune; Vikram Sinha; Lynne Yao
Journal:  Pediatr Clin North Am       Date:  2017-12       Impact factor: 3.278

Review 2.  Surrogate Endpoints in Pediatric Studies Submitted to the US FDA.

Authors:  Dionna J Green; Haihao Sun; Janelle Burnham; Xiaomei I Liu; John van den Anker; Jean Temeck; Lynne Yao; Susan K McCune; Gilbert J Burckart
Journal:  Clin Pharmacol Ther       Date:  2018-08-09       Impact factor: 6.875

Review 3.  Design and conduct of early phase drug studies in children: challenges and opportunities.

Authors:  Michael Rieder; Daniel Hawcutt
Journal:  Br J Clin Pharmacol       Date:  2016-08-08       Impact factor: 4.335

Review 4.  Moving toward a paradigm shift in the regulatory requirements for pediatric medicines.

Authors:  William Wei Lim Chin; Angelika Joos
Journal:  Eur J Pediatr       Date:  2016-09-19       Impact factor: 3.183

5.  Primary Endpoints in Pediatric Efficacy Trials Submitted to the US FDA.

Authors:  Dionna J Green; Janelle M Burnham; Paul Schuette; Xiaomei I Liu; Brian M Maas; Lynne Yao; Susan K McCune; Joseph Chen; John N van den Anker; Gilbert J Burckart
Journal:  J Clin Pharmacol       Date:  2018-04-17       Impact factor: 3.126

6.  Stratification, Hypothesis Testing, and Clinical Trial Simulation in Pediatric Drug Development.

Authors:  Ann W McMahon; Kevin Watt; Jian Wang; Dionna Green; Ram Tiwari; Gilbert J Burckart
Journal:  Ther Innov Regul Sci       Date:  2016-06-02       Impact factor: 1.778

7.  Enrichment Strategies in Pediatric Drug Development: An Analysis of Trials Submitted to the US Food and Drug Administration.

Authors:  Dionna J Green; Xiaomei I Liu; Tianyi Hua; Janelle M Burnham; Robert Schuck; Michael Pacanowski; Lynne Yao; Susan K McCune; Gilbert J Burckart; Issam Zineh
Journal:  Clin Pharmacol Ther       Date:  2018-02-13       Impact factor: 6.875

Review 8.  Exposure Matching of Pediatric Anti-infective Drugs: Review of Drugs Submitted to the Food and Drug Administration for Pediatric Approval.

Authors:  Kanecia Zimmerman; Martin Putera; Christoph P Hornik; P Brian Smith; Daniel K Benjamin; Yeruk Mulugeta; Gilbert J Burckart; Michael Cohen-Wolkowiez; Daniel Gonzalez
Journal:  Clin Ther       Date:  2016-06-28       Impact factor: 3.393

Review 9.  Pharmacokinetics of nanotechnology-based formulations in pediatric populations.

Authors:  Venkata K Yellepeddi; Andrea Joseph; Elizabeth Nance
Journal:  Adv Drug Deliv Rev       Date:  2019-09-05       Impact factor: 15.470

Review 10.  Developmental Pharmacodynamics and Modeling in Pediatric Drug Development.

Authors:  Laurie S Conklin; Eric P Hoffman; John van den Anker
Journal:  J Clin Pharmacol       Date:  2019-09       Impact factor: 3.126

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