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Alexion Announces Successful Phase 3 PREVENT Study of SolirisĀ® (Eculizumab) in Patients with Neuromyelitis Optica Spectrum Disorder (NMOSD)
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Alexion (ALXN)Says Selection of Positive Phase 3 Clinical Data for ALXN1210 in Patients with PNH for Late-Breaking Oral Presentation at EHA
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Results of Phase 1b/2 Dose Regimen Optimization Studies for ALXN1210 in Patients with Paroxysmal Nocturnal Hemoglobinuria (PNH) Presented at American Society of Hematology (ASH) Meeting
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Alexion Pharma (ALXN) Announces Interim Analysis from Phase 3 Open-Label Extension Study Shows Sustained Benefits of Soliris (Eculizumab) Treatment
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Alexion Receives Positive CHMP Opinion for SolirisĀ® (Eculizumab) for the Treatment of Patients with Refractory Generalized Myasthenia Gravis (gMG) in the European Union
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Alexion Pharma (ALXN) Says Data from Global aHUS Registry Shows Reduced Risk with Soliris
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Alexion Pharma (ALXN) Granted Ophand Drug Status in Europe for ALXN1210
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