The European Medicines Agency is set to decide this week whether to recommend for approval what could become Europe’s first treatment for neuromyelitis optica spectrum disorder (NMOSD) –Alexion Pharmaceuticals’ monoclonal antibody Soliris (eculizumab).
In addition, the EMA is expected to decide whether to fast track the planned marketing authorization application (MAA) for another product targeting the condition – satralizumab, the recycling antibody that...
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