Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
3282595 | Clinical Gastroenterology and Hepatology | 2014 | 12 Pages |
Abstract
Despite a relevant mechanism of action, ASP9831 did not significantly alter the biochemical markers of NASH, compared with placebo, in a clinical trial. This highlights the difficulties of developing therapeutics for NASH and the need for more extensive preclinical testing of mechanisms of potential drug candidates. Clinicaltrialsregister.eu: 2005-001687-31; EudraCT numbers: 2007-002114-19.
Keywords
CmaxTNFPDE4methionine-choline deficientMCDtmaxALTPDELPSAUCcAMPTEAEadenosine 3′,5′-cyclic monophosphateASTAspartate aminotransferaseAlanine aminotransferasenonalcoholic steatohepatitisTherapeutic targetsFatty liver diseasemaximum drug concentrationTreatmentadverse eventtreatment-emergent adverse eventtumor necrosis factorPhosphodiesteraselipopolysaccharideNash
Related Topics
Health Sciences
Medicine and Dentistry
Gastroenterology
Authors
Vlad Ratziu, Pierre Bedossa, Sven M. Francque, Dominique Larrey, Guruprasad P. Aithal, Lawrence Serfaty, Mihai Voiculescu, Liliana Preotescu, Frederik Nevens, Victor De Lédinghen, Gabriele I. Kirchner, Pavel Trunecka, Stephen D. Ryder,