DNDN - Dendreon: FDA To Amend SPA For Phase III Trial Of Provenge
By Saba Ali Last update: 7:52 a.m. EDT March 12, 2008
Dendreon Corp. (DNDN) said the Food and Drug Administration agreed to amend Special Protocol Assessment for the Phase III IMPACT clinical trial of Provenge, cellular immunotherapy for the treatment of advanced prostate cancer. The Seattle biopharmaceutical company said the amended SPA accelerates the expected timing of the final IMPACT results by about one year.
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