Top Regulatory News Stories – Week Ending November 16, 2018

The FDA granted accelerated approval to Merck’s checkpoint immunotherapy pembrolizumab (Keytruda) for the treatment of certain patients with advanced hepatocellular carcinoma (HCC), the most common form of liver cancer. https://www.cancerresearch.org/blog/november-2018/fda-approves-pembrolizumab-hcc-liver-cancer   Exelixis, Inc. announced that its partner IPSEN received approval from the European Commission for CABOMETYX (cabozantinib) tablets as a monotherapy for hepatocellular carcinoma in[…]