Brexpiprazole filed with EMA for adult patients with schizophrenia
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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