With Bristol-Myers Squibb Co.’s checkpoint inhibitor Opdivo (nivolumab) having a US FDA PDUFA date of Sept. 24, 2017, for use as a second-line therapy for hepatocellular carcinoma (HCC), and Eisai Co. Ltd.'s oral multiple receptor tyrosine kinase inhibitor, lenvatinib, submitted for US and European approval as first-line HCC therapy, announced on July 25, changes are afoot in this therapeutic area. (Also see "Lenvatinib HCC Results Give Sorafenib Cause To REFLECT?" - Scrip, 6 June, 2017.)
One change has just occurred: on Aug. 7, the German multinational Bayer AG announced the EU approval of Stivarga...
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