Exelixis Inc. completed its submission of a supplemental new drug application (sNDA) for US FDA accelerated approval of Cabometyx (cabozantinib) in previously untreated advanced renal cell carcinoma (RCC) on Aug. 16, a day after the drug's competitive position was bolstered by disappointing interim Phase III results for Bristol-Myers Squibb Co.'s Opdivo (nivolumab) and Yervoy (ipilimumab).
South San Francisco-based Exelixis is seeking early approval for its tyrosine kinase inhibitor (TKI) – which blocks MET, AXL and...








