Soliris (eculizumab) goedgekeurd door FDA voor alle patinten met atypisch hemolytisch uremisch syndroom (aHUS)

Health and Fitness Health and Fitness

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Soliris (eculizumab) goedgekeurd door FDA voor al .. met atypisch hemolytisch uremisch syndroom (aHUS)

Soliris (eculizumab) goedgekeurd door FDA voor alle patinten met atypisch hemolytisch uremisch syndroom (aHUS)

^{Published on 2011-09-23 12:22:42 - Market Wire}

CHESHIRE, Conn.--([ BUSINESS WIRE ])--Alexion Pharmaceuticals, Inc. (Nasdaq: ALXN) meldt dat de U.S. Food and Drug Administration (FDA) Soliris (eculizumab) heeft goedgekeurd voor de behandeling van patinten van alle leeftijden met atypisch hemolytisch uremisch syndroom (aHUS). Dit betreft de eerste goedgekeurde behandeling van deze ziekte. aHUS is een uiterst zeldzame, levensbedreigende genetische kwaal, die de organen een voor een aantast, hetgeen leidt tot beroerte, hartaanval, nierfalen en uiteindelijk de dood. Alexion houdt op maandag 26 september om 15:00 uur Nederlandse tijd een conference call /webcast ter bespreking van de FDA-goedkeuring.

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