(ENTA)—ABBV still hasn’t used its FDA priority review voucher purchased for $350M in Aug 2015 (#msg-116321586). IMO, it’s becoming more and more likely ABBV will use it for the ABT-493/ABT-530 pan-genotypic HCV regimen, which has six phase-3 trials in progress (#msg-119900756).
“The efficient-market hypothesis may be the foremost piece of B.S. ever promulgated in any area of human knowledge!”
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