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The EMA Committee for Medicinal Products for Human Use CHMP has recommended approval of the marketing authorization for Daklinza daclatasvir in combination with other medicines for the treatment of hepatitis C. chronic in adults, indicates a press release from the EMA. This drug belongs to the new class of direct-acting antivirals DAAs, including the very expensive sofosbuvir Gilead. DAAs are revolutionizing the treatment of hepatitis C, underlines the EMA, which specifies that it вactively supports the development of these new therapeutic optionsв. This green light must now be formally approved by the European Commission. Mais lвun des problГЁmes au Niger excedrin la disponibilitГ impalamycin tests de diagnostique rapide TDR.

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