Altuviiio May See Rapid Uptake Upon European Approval In Hemophilia A
Pediatric Data Clears Path For EMA Filing
Sanofi announced results from its XTEND-Kids trial, clearing the last requirement before an anticipated second half filing for Altuviiio’s approval with the EMA.
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Phase III success for efanesoctocog alfa sets up a filing in the near future, and a chance to seize market share from existing Factor VIII products, as well as Roche’s Hemlibra.
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