Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
BUSINESS
Lenvima-Keytruda Combo Earns FDA’s Breakthrough Designation for RCC
The US FDA has granted Breakthrough Therapy designation for a combination therapy pairing Eisai’s multi-kinase inhibitor Lenvima (lenvatinib) and US Merck’s PD-1 inhibitor Keytruda (pembrolizumab) for the treatment of advanced/metastatic renal cell carcinoma (RCC), the two companies said on January…
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