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Minerva Neurosciences Inc. said Monday that it received a refusal to file letter from the Food and Drug Administration for its application for roluperidone as a treatment for patients with schizophrenia. “The company intends to request a Type A meeting and looks forward to continued discussions with the FDA,” Minerva CEO said in a news release. Minerva’s stock has soared 109.6% so far this year, while the broader S&P 500 has declined 24.8%.
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