Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
BUSINESS
Nippon Shinyaku Seeks US Approval for DMD Therapy Viltolarsen
Nippon Shinyaku said on October 2 that it has completed the rolling submission of its oligonucleotide Duchenne muscular dystrophy (DMD) drug viltolarsen with the US FDA, which is expected to accept the application within 60 days according to a typical…
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