Butler Javed, Fonarow Gregg C, O'Connor Christopher, Adams Kirkwood, Bonow Robert O, Cody Robert J, Collins Sean P, Dunnmon Preston, Dinh Wilfried, Fiuzat Mona, Georgiopoulou Vasiliki V, Grant Stephen, Kim So-Young, Kupfer Stuart, Lefkowitz Martin, Mentz Robert J, Misselwitz Frank, Pitt Bertram, Roessig Lothar, Schelbert Erik, Shah Monica, Solomon Scott, Stockbridge Norman, Yancy Clyde, Gheorghiade Mihai
Cardiology Division, Stony Brook University, Stony Brook, NY.
University of California, Los Angeles, CA.
Am Heart J. 2015 Mar;169(3):305-14. doi: 10.1016/j.ahj.2014.12.001. Epub 2014 Dec 17.
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.
医学疗法的进步带来了更好的患者治疗效果,这在很大程度上与临床试验的成功开展有关,临床试验能提供有关新干预措施疗效和安全性的关键信息。然而,在美国开展临床试验在受试者招募和保留方面仍面临越来越多的挑战。这些趋势与向更多跨国试验的转变并行,在跨国试验中,大多数受试者是在美国以外的国家招募的,这使得试验结果对美国人群的普遍适用性受到质疑。本文介绍了临床医生、研究人员、申办者和监管者的观点及建议,他们参加了由美国食品药品监督管理局组织的一次会议,旨在改善美国目前的临床试验趋势。