Serelaxin appers to be dead in the water. The FDA rejected it in May 2014 (#msg-102108200) following a negative advisory panel (#msg-99602449). The European MAA was also withdrawn.
This case is a reminder that BTD (which Serelaxin had) does not ensure regulatory success.
“The efficient-market hypothesis may be the foremost piece of B.S. ever promulgated in any area of human knowledge!”
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