Corcept Therapeutics saw its stock price cut in half after the company revealed in its first quarter earnings report that mifepristone failed to achieve the primary endpoint in a Phase III clinical trial for the treatment of psychotic depression.
The glucocorticoid receptor antagonist Korlym (mifepristone 300mg) was approved in the US to treat patients with Cushing's syndrome in 2012, but Menlo Park, California-based Corcept was testing a once-daily 1,200mg dose of mifepristone in psychotic depression (scripintelligence.com, 20 February 2012)
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