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About CTRP

NCI's Clinical Trials Reporting Program (CTRP) fulfills a recommendation made by the NCI Clinical Trials Working Group (CTWG) to the National Cancer Advisory Board. The purpose of the program is to establish a comprehensive database containing regularly updated information on all NCI-funded clinical trials. Grantees enter specific information about each clinical trial into the database. NCI internally transfers to CTRP information on CTEP, CCR and DCP trials, eliminating the need for awardees to enter information on these trials. NCI uses this information to coordinate research efforts to optimize our nation's investment in cancer research. NCI initiated a phased launch of CTRP, which started January 2009, with a focus on registering interventional trials only. The registration of observational, ancillary and correlative studies will begin at a later date.

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