Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
BUSINESS
US FDA Gives 1st Nod for Lenvima/Keytruda Combo as 2nd-Line Therapy for Endometrial Carcinoma
The US FDA approved on September 17 the combination therapy of Eisai’s multi-kinase inhibitor Lenvima (lenvatinib) plus US Merck’s PD-1 inhibitor Keytruda (pembrolizumab) for the treatment of patients with advanced endometrial carcinoma, marking the first approval for the combo, the…
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