| Literature DB >> 28356300 |
Javed Butler1, Carine E Hamo2, James E Udelson2, Christopher O'Connor2, Hani N Sabbah2, Marco Metra2, Sanjiv J Shah2, Dalane W Kitzman2, John R Teerlink2, Harold S Bernstein2, Gabriel Brooks2, Christophe Depre2, Mary M DeSouza2, Wilfried Dinh2, Mark Donovan2, Regina Frische-Danielson2, Robert J Frost2, Dahlia Garza2, Udo-Michael Gohring2, Jennifer Hellawell2, Judith Hsia2, Shiro Ishihara2, Patricia Kay-Mugford2, Joerg Koglin2, Marc Kozinn2, Christopher J Larson2, Martha Mayo2, Li-Ming Gan2, Pierrre Mugnier2, Sekayi Mushonga2, Lothar Roessig2, Cesare Russo2, Afshin Salsali2, Carol Satler2, Victor Shi2, Barry Ticho2, Michael van der Laan2, Clyde Yancy2, Norman Stockbridge2, Mihai Gheorghiade2.
Abstract
The increasing burden and the continued suboptimal outcomes for patients with heart failure underlines the importance of continued research to develop novel therapeutics for this disorder. This can only be accomplished with successful translation of basic science discoveries into direct human application through effective clinical trial design and execution that results in a substantially improved clinical course and outcomes. In this respect, phase II clinical trials play a pivotal role in determining which of the multitude of potential basic science discoveries should move to the large and expansive registration trials in humans. A critical examination of the phase II trials in heart failure reveals multiple shortcomings in their concept, design, execution, and interpretation. To further a dialogue on the challenges and potential for improvement and the role of phase II trials in patients with heart failure, the Food and Drug Administration facilitated a meeting on October 17, 2016, represented by clinicians, researchers, industry members, and regulators. This document summarizes the discussion from this meeting and provides key recommendations for future directions.Entities:
Keywords: United States Food and Drug Administration; clinical trial; heart failure; mortality; safety
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Year: 2017 PMID: 28356300 PMCID: PMC5400283 DOI: 10.1161/CIRCHEARTFAILURE.116.003800
Source DB: PubMed Journal: Circ Heart Fail ISSN: 1941-3289 Impact factor: 8.790