Abstract
There has been considerable interest of late in increasing the transparency of clinical trials, including increasing access to the raw data from trials sponsored by the pharmaceutical industry.(1) Since May 2013, investigators have been able to request access to deidentified patient-level data from clinical trials sponsored by GlaxoSmithKline,(2) subject to review and oversight by an independent review panel (https://clinicalstudydatarequest.com/Default.aspx). As the members of this panel, we now have more than 12 months of experience with this initiative - and can report that it has been a productive and successful first step. The system was launched on May 7, 2013, and . . .
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Chertow, D. S., Kleine, C., Edwards, J. K., Scaini, R., Giuliani, R., & Sprecher, A. (2014). Ebola Virus Disease in West Africa — Clinical Manifestations and Management. New England Journal of Medicine, 371(22), 2054–2057. https://doi.org/10.1056/nejmp1413084
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