Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
BUSINESS
Takeda’s Mobocertinib Bags FDA Breakthrough Therapy Status for EGFR Exon 20 Mutant NSCLC
Takeda Pharmaceutical said on April 27 that it has won breakthrough therapy status from the US FDA for its investigational tyrosine kinase inhibitor (TKI) mobocertinib (TAK-788) for non-small cell lung cancer (NSCLC) with EGFR exon 20 insertion mutations. The designation…
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Japan’s Central Social Insurance Medical Council (Chuikyo) on November 5 approved the reimbursement listing for a slate of new medicines,…
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Japan’s all-important reimbursement policy panel on December 20 approved an outline of drug pricing reforms for FY2024, which enshrines a…