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Gentium unlikely to get CHMP recommendation for defibrotide use in Hepatic Veno-Occlusive disease

Read time: 1 mins
Last updated:22nd Feb 2013
Published:22nd Feb 2013
Source: Pharmawand

Gentium S.p.A. had presented an oral explanation at the EMA Committee for Medicinal Products for Human Use ("CHMP") as part of its Marketing Authorization Application for Defibrotide to treat and prevent Hepatic Veno-Occlusive disease in adults and children undergoing hematopoietic stem cell transplantation therapy. Following the oral explanation,based on preliminary feedback from the CHMP,the Company expects an opinion recommending against approval of the Marketing Authorization Application for Defibrotide to treat and prevent Hepatic Veno-Occlusive disease in adults and children undergoing hematopoietic stem cell transplantation therapy.

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