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Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/17782

Title: Surrogate endpoints: application in pediatric clinical trials
Authors: MOLENBERGHS, Geert
Issue Date: 2013
Publisher: Wiley-Blackwell
Citation: Mulberg, A.; Murphy, D.; Dunne, J.; Mathis, L.L. (Ed.). Pediatric Drug Development: Concepts and Applications, p. 530-538
Abstract: This chapter examines the use of surrogate endpoints in clinical research in general and the role that they can play in pediatric research in particular. A surrogate endpoint does not directly measure clinical impact, but rather reflects the desired therapeutic treatment effect. With the anticipated increase in pediatric clinical trials, the need for surrogate endpoints will increase concomitantly. One must proceed cautiously to ensure that the selection of surrogate endpoints is based on sound scientific rationales. Noted failures of surrogate endpoints to assess treatment effects adequately in adults must not be repeated in pediatric clinical trials, and the concern over inadequately assessing the benefit risk ratio with a surrogate endpoint is of even greater concern in the pediatric population. Trial designs should facilitate the evaluation of proposed surrogate endpoints, including standardizing collection methods and the frequency of biomarker measurements, to allow for across-study analyses to be performed.
URI: http://hdl.handle.net/1942/17782
DOI: 10.1002/9781118312087.ch41
ISBN: 9781118312155
Category: B2
Type: Book Section
Validation: vabb, 2016
Appears in Collections: Research publications

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