| Literature DB >> 25728719 |
Javed Butler1, Gregg C Fonarow2, Christopher O'Connor3, Kirkwood Adams4, Robert O Bonow5, Robert J Cody6, Sean P Collins7, Preston Dunnmon8, Wilfried Dinh9, Mona Fiuzat3, Vasiliki V Georgiopoulou10, Stephen Grant8, So-Young Kim11, Stuart Kupfer12, Martin Lefkowitz13, Robert J Mentz3, Frank Misselwitz11, Bertram Pitt14, Lothar Roessig11, Erik Schelbert15, Monica Shah16, Scott Solomon17, Norman Stockbridge8, Clyde Yancy18, Mihai Gheorghiade5.
Abstract
Advances in medical therapies leading to improved patient outcomes are in large part related to successful conduct of clinical trials that offer critical information regarding the efficacy and safety of novel interventions. The conduct of clinical trials in the United States, however, continues to face increasing challenges with recruitment and retention. These trends are paralleled by an increasing shift toward more multinational trials where most participants are enrolled in countries outside the United States, bringing into question the generalizability of the results to the American population. This manuscript presents the perspectives and recommendations from clinicians, researchers, sponsors, and regulators who attended a meeting facilitated by the Food and Drug Administration to improve upon the current clinical trial trends in the United States.Entities:
Mesh:
Year: 2014 PMID: 25728719 DOI: 10.1016/j.ahj.2014.12.001
Source DB: PubMed Journal: Am Heart J ISSN: 0002-8703 Impact factor: 4.749