Changes in drug development regulations and their impact on clinical trials

Published

Book Section

© Springer International Publishing AG 2018. Regulatory changes in the United States and Europe have stimulated major pediatric clinical trials of over 15 different antihypertensive agents over the last two decades. With increased pediatric hypertension trial experience, trial designs have been refined, andwe now better understand factors associated with trial success or failure. Appropriate dose range, weight-based dosing, use of a liquid formulation, and use of appropriate blood pressure endpoints are all factors that have been associated with improved trial success. These lessons learned and important modifications in trial design templates are reflected in the United States Food andDrug Administration Written Request criteria. The Written Request provides valuable information that can be used to optimally design future clinical trials of antihypertensive agents as well as other therapeutic agents for use in children.

Full Text

Duke Authors

Cited Authors

  • Hill, KD; Török, RD; Portman, RJ; Li, JS

Published Date

  • January 1, 2018

Book Title

  • Pediatric Hypertension

Start / End Page

  • 841 - 852

International Standard Book Number 13 (ISBN-13)

  • 9783319311067

Digital Object Identifier (DOI)

  • 10.1007/978-3-319-31107-4_38

Citation Source

  • Scopus