Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
BUSINESS
Sanofi Files for Subcutaneous Formulation of Sarclisa in Japan
Sanofi said on August 28 that it has filed for regulatory approval of a subcutaneous formulation of its anti-CD38 antibody Sarclisa (isatuximab) in Japan. The application covers use in combination with pomalidomide/dexamethasone, carfilzomib/dexamethasone, and bortezomib/lenalidomide/dexamethasone for the treatment of multiple…
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