That’s what was going on here, but the FDA just shot a hole in Teva’s plan.
Teva’s fallback position on defending the Copaxone franchise will now pass to the thrice-weekly 40mg formulation, which is being tested in a trial called GALA that is expected to report top-line data in late 2012 and the complete dataset in mid 2014 (#msg-57549803).
“The efficient-market hypothesis may be the foremost piece of B.S. ever promulgated in any area of human knowledge!”
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