US FDA moves approval goalposts for GSK/Valeant's ezogabine and Eisai's eribulin; Abbott/Eisai's Humira filed for additional indication in Japan
1 September 2010
The US Food and Drug Administration disappointed several companies yesterday by moving the goalposts for approving their drugs by around three months by extending the Prescription Drug User Fee Act (PDUFA) dates for their review.
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