Alexion wins FDA OK in aHUS; CHMP also gives thumbs up
This article was originally published in Scrip
Executive Summary
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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