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February 28, 2013
09:28 EDTRPRXRepros granted end of Phase 2 meeting in late May for Proellex-V by FDA
Repros Therapeutics announced that the FDA has agreed to a Type B meeting scheduled for the last half of May to discuss the Phase 3 development of Proellex as a vaginally administered product for the treatment of uterine fibroids. During the meeting, Repros will discuss the proposed plans for a Phase 3 study, the FDA's requirements for the size of the safety population and the adequacy of the already completed preclinical studies to support a marketing application. Once the meeting is held, the company will report the outcome to the financial community in a timely fashion.
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July 29, 2014
11:37 EDTRPRXHigh option volume stocks
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