Alexion wins FDA OK in aHUS; CHMP also gives thumbs up
This article was originally published in Scrip
Alexion Pharmaceuticals on 23 September won the US FDA's blessing to expand the indication for Soliris (eculizumab), a first-in-class terminal complement inhibitor, as a treatment for patients with atypical hemolytic uremic syndrome (aHUS), a chronic, ultra-rare disease characterized by the formation of blood clots in small blood vessels throughout the body.
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