Gentium announces NDA submission for Defibrotide
theflyonthewall
On Wednesday July 6, 2011, 7:35 am EDT
Gentium S.p.A. announced that it has submitted a New Drug Application, NDA, to the United States Food and Drug Administration, FDA, for Defibrotide for the treatment of hepatic veno-occlusive disease, VOD, in adults and children undergoing hematopoietic stem-cell transplantation, HSCT.
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