Market ExpansionBiogen partner Eisai's request for the EMA's CHMP to reexamine the MAA for lecanemab in amyloid-positive early Alzheimer's disease has paid off with a positive recommendation, preserving the majority of the addressable patient population - approximately 85-90%.
Product DifferentiationFelzartamab is expected to be a differentiated product in IgAN and a solid early entrant in pMN and AMR, with the potential for over $5 billion in peak sales opportunities.
Regulatory ApprovalThe EMA announced a positive CHMP recommendation to approve Leqembi in the EU, overturning the negative opinion first issued.