US FDA accepts NDAs from Genentech, Eisai, GSK and S-P
l US biotechnology major Genentech has completed the submission of a supplemental Biologics License Application to the Food and Drug Administration for use of Herceptin (trastuzumab) to treat early-stage, human epidermal growth factor receptor 2-positive breast cancer. The firm has requested a priority review from the FDA which, if granted, requires action within six months.
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