4′-azido, 3′-fluoro substituted nucleoside derivatives as inhibitors of HCV RNA replication
Abstract:
The present invention relates to the use of 3′-fluoro, 4′-azido nucleoside phosphoramidate prodrug derivatives of formula I wherein the symbols are as defined in the specification, to pharmaceutically acceptable salts thereof, and to pharmaceutical compositions containing such compounds for the treatment of HCV.
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