- The FDA notifies Repros Therapeutics (NASDAQ:RPRX) that it may proceed with phase 1 and phase 2 studies for Proellex under separate INDs for endometriosis and uterine fibroids while remaining on partial clinical hold.
- The maximum allowed dose will be 12 mg daily.
- Consensus 2015 revenue estimate is $16.8M.
- 133 mutual funds have positions, up from 120 a year earlier.
Repros gets the nod to proceed in clinical trials
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