June 2007
Worldwide Biotech;Jun2007, Vol. 19 Issue 6, p5
Trade Publication
The article reports that the Committee for Human Medicinal Products of the European Medicines Agency has adopted a positive opinion recommending marketing authorization for Soliris, a drug from Alexion Pharmaceuticals Inc. The drug is for patients with paroxysmal nocturnal hemoglobinuria (PNH). Soliris is intended to reduce hemolysis in patients with PNH. The committee evaluated Soliris under the European Accelerated Assessment procedure.


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