Cubist
Pharmaceuticals CBST today announced that the U.S.
Food and Drug Administration (FDA) has accepted the Company's New Drug
Application (NDA) for its investigational antibiotic tedizolid phosphate
(TR-701) with Priority Review. The FDA has assigned a Prescription Drug
User Fee Act (PDUFA) action date of June 20, 2014. Cubist is seeking FDA
approval of tedizolid for the treatment of acute bacterial skin and skin
structure infections (ABSSSI).
See full press release
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