کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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5121905 | 1486849 | 2016 | 6 صفحه PDF | دانلود رایگان |
ObjectiveThe study aimed to characterize the public availability of pivotal clinical trial results for newly approved drugs.Study Design and SettingWe examined the availability of pivotal clinical trial results for new molecular entities (NMEs) approved by the US Food and Drug administration (FDA) from 2009 to 2013. For each NME, we quantified the time from approval date until results were available on the FDA web site, in the ClinicalTrials.gov basic results database, and in a medical journal.ResultsTwo hundred fifty-five pivotal trials supporting 88 NMEs met our criteria. The median time until pivotal trial results were available on the FDA web site, ClinicalTrials.gov, and in a publication was 42Â days, 27Â days, and â28Â days, respectively. In the first 30Â days after approval, 52% of pivotal trials were summarized in ClinicalTrials.gov, 20% were posted to the FDA web site, and 46% were published in a journal. Across all sources, 79% of pivotal trials had results available within 30Â days of approval. From 2009 to 2013, the average time until public availability has improved for federal sources.ConclusionsPivotal trials of newly approved drugs appeared first in publications. Results from most pivotal trials were publicly available in some source within 30Â days of approval.
Journal: Journal of Clinical Epidemiology - Volume 77, September 2016, Pages 78-83