Keywords: fda, approves, alexion, soliris, paroxysmal, nocturnal, hemogobinuria
FDA approves Alexion's Soliris for paroxysmal nocturnal hemogobinuria
Article | 26 March 2007
USA-based biotechnology company Alexion Pharmaceuticals says that the Food and Drug Administration's approval of its drug Soliris (eculizumab), as a ...
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