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The FDA accepted a new drug application for BioXcel Therapeutics' novel, orally dissolving thin film formulation of dexmedetomidine BXCL501 for the acute treatment of agitation associated with schizophrenia and bipolar disorders I and II, based on the phase III SERENITY trials presented at this year's American Psychiatric Association meeting.
Many state medical board license applications do not follow national recommendations aimed at protecting physicians' mental health -- as only one state, North Carolina, has fully adopted the Federation of State Medical Boards' recommendations. (
JAMA)
The FDA gave the green light to PharmaTher Holdings to evaluate ketamine in the treatment of levodopa-induced dyskinesia in patients with Parkinson's disease in a phase II trial.