Novel end points for clinical trials in young children with cystic fibrosis

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Novel end points for clinical trials in young children with cystic fibrosis

Cystic fibrosis (CF) lung disease commences early in the disease progression and is the most common cause of mortality. While new CF disease-modifying agents are currently undergoing clinical trial evaluation, the implementation of such trials in young children is limited by the lack of age-appropri...

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Bibliographic Details
Main Authors:	Simpson, S., Mott, L., Esther, C., Stick, S., Hall, Graham
Format:	Journal Article
Published:	Expert Reviews Ltd 2013
Online Access:	http://hdl.handle.net/20.500.11937/54974

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