| Literature DB >> 30658732 |
Philippe Mathurin1, Mark Thursz2.
Abstract
In some areas of medicine the clinical development pathway through phase II and III clinical trials has been well mapped out and refined through extensive experience. In contrast, a number of key questions remain unanswered in the development of novel therapeutics for alcoholic hepatitis. The use of mortality as an endpoint in phase II clinical trials will potentially restrict the appeal of this therapeutic area for pharmaceutical companies, as the number of patients required for adequately powered clinical trials becomes impractical. Herein, we discuss alternative endpoints and conclude that dynamic assessment of liver function is the most pragmatic option in early stage studies. Stratification based on disease severity should be applied to avoid uneven distribution of patients with substantially differing mortality risks. Consensus on early phase trial design would help to facilitate new therapeutic development in this area of high unmet medical need.Entities:
Keywords: ABIC; GAHS; Infection; MELD; Surrogate endpoints
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Year: 2019 PMID: 30658732 DOI: 10.1016/j.jhep.2018.11.005
Source DB: PubMed Journal: J Hepatol ISSN: 0168-8278 Impact factor: 25.083