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Avexa and Progen Merger Update
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XenoPort Announces $40 Million Registered Direct Financing
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Samenvatting: Europese Commissie verleent VIDAZA volledige marktautorisatie voor behandeling van patinten met een hoger risico


//health-fitness.news-articles.net/content/2008/ .. handeling-van-patinten-met-een-hoger-risico.html
Published in Health and Fitness on Wednesday, December 24th 2008 at 9:20 GMT, Last Modified on 2008-12-24 09:21:05 by Market Wire   Print publication without navigation


BOUDRY, Zwitserland--([ BUSINESS WIRE ])--Celgene International Sàrl (Nasdaq:CELG) maakt bekend dat de eerste en enige epigenetische kankertherapie een significante overlevingsverlenging toont voor patiënten met Intermediate-2 en hoger-risico MDS en AML. De Europese Commissie verleent VIDAZA van Celgene volledige marktautorisatie voor behandeling van patiënten met een hoger risico voor myelodysplastische syndromen en acute myeloid leukemia. Deze eerste goedgekeurde therapie is zowel effectief voor een brede range van MDS subgroepen als voor Acute Myeloid Leukaemia (AML).

Deze bekendmaking is officieel geldend in de originele brontaal. Vertalingen zijn slechts als leeshulp bedoeld en moeten worden vergeleken met de tekst in de brontaal welke als enige, juridische geldigheid beoogt.


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