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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