Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
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Enhertu Now under US Review for Post-Neoadjuvant HER2 Breast Cancer
Daiichi Sankyo said on March 9 that the US FDA has accepted for review a supplemental biologics license application for its anti-HER2 antibody drug conjugate (ADC) Enhertu (trastuzumab deruxtecan) seeking a new indication in HER2-positive early breast cancer. The company…
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