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The 64 mg and 32 mg doses were not statistically significantly different from placebo at Week 12 on the primary endpoint, the PANSS Marder Negative Symptoms Factor Score (p 0.064 and 0.259, respectively), or the key secondary endpoint, the Personal and Social Performance Scale Total Score (p 0.021 and p 0.542, respectively)Roluperidone separated from placebo on both primary and key secondary endpoints at Weeks 4, 8 and 12Roluperidone was generally well tolerated with a safety profile comparable to placebo
WALTHAM, Mass., May 29, 2020 (GLOBE NEWSWIRE) -- Minerva Neurosciences, Inc. (NASDAQ: NERV), a... More

