Brexpiprazole filed with EMA for adult patients with schizophrenia

23 March 2017
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The European Medicines agency is expected to complete its review of brexpiprazole for use in schizophrenia, according to the drug’s developers.

Danish CNS specialist Lundbeck (LUND: CO) and Japan’s Otsuka Pharmaceutical (TYO: 4768) today announced that the EMA has accepted for review a Marketing Authorization Application for brexpiprazole to treat schizophrenia in adults.

Brexpiprazole is a once-daily, second-generation (atypical) oral antipsychotic that was discovered by Otsuka and co-developed by Otsuka and Lundbeck. The mechanism of action for brexpiprazole in the treatment of schizophrenia is unknown. However, the efficacy of brexpiprazole may be mediated through a combination of partial agonist activity at serotonin 5-HT1A and dopamine D2 receptors, and antagonist activity at serotonin 5-HT2A receptors. In addition, brexpiprazole exhibits high affinity (subnanomolar) for these receptors as well as for noradrenaline alpha1B/2C receptors.

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