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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The Wednesday TableShe had been on virtual calls since eight in the morning. The screen glowed. Her eyes burned. Plugged into Teams across time zones, she was digitally connected yet entirely isolated from the reality of Japan’s pharma market.She needed…





