Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/62807
Title: Optimizing Clinical Trial Design to Maximize Evidence Generation in Pediatric HIV
Authors: Deborah Ford
Rebecca Turner
Anna Turkova
Martina Penazzato
Victor Musiime
Mutsa Bwakura-Dangarembizi
Avy Violari
Chishala Chabala
Thanyawee Puthanakit
Tavitiya Sudjaritruk
Tim R. Cressey
Marc Lallemant
Diana M. Gibb
Keywords: Medicine
Issue Date: 15-Aug-2018
Abstract: For HIV-infected children, formulation development, pharmacokinetic (PK) data, and evaluation of early toxicity are critical for licensing new antiretroviral drugs; direct evidence of efficacy in children may not be needed if acceptable safety and PK parameters are demonstrated in children. However, it is important to address questions where adult trial data cannot be extrapolated to children. In this fast-moving area, interventions need to be tailored to resource-limited settings where most HIV-infected children live and take account of decreasing numbers of younger HIV-infected children after successful prevention of mother-to-child HIV transmission. Innovative randomized controlled trial (RCT) designs enable several questions relevant to children's treatment and care to be answered within the same study. We reflect on key considerations, and, with examples, discuss the relative merits of different RCT designs for addressing multiple scientific questions including parallel multi-arm RCTs, factorial RCTs, and cross-over RCTs. We discuss inclusion of several populations (eg, untreated and pretreated children; children and adults) in "basket" trials; incorporation of secondary randomizations after enrollment and use of nested substudies (particularly PK and formulation acceptability) within large RCTs. We review the literature on trial designs across other disease areas in pediatrics and rare diseases and discuss their relevance for addressing questions relevant to HIV-infected children; we provide an example of a Bayesian trial design in prevention of mother-to-child HIV transmission and consider this approach for future pediatric trials. Finally, we discuss the relevance of these approaches to other areas, in particular, childhood tuberculosis and hepatitis.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85055149780&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/62807
ISSN: 19447884
Appears in Collections:CMUL: Journal Articles

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