Perospirone is an atypical antipsychotic agent for the treatment of schizop
hrenia. Its primary mode of action is through antagonism of serotonin 5-HT2
A and dopamine D-2 receptors.
An 8-week course of oral perospirone 8 to 48 mg/day displayed efficacy in u
p to 75% of patients with schizophrenia participating in phase II and phase
III trials. The onset of action of the drug was about 2 weeks.
Perospirone was effective against positive, negative and general symptoms i
n patients with schizophrenia, as assessed with standard rating scales (Bri
ef Psychiatric Rating Scale, Positive and Negative Symptom Scale).
Compared with haloperidol 2 to 12 mg/day, perospirone 8 to 48 mg/day was si
gnificantly more effective against negative symptoms and tended to be more
effective against general symptoms and most positive symptoms in a trial in
145 patients with schizophrenia. Perospirone had efficacy similar to that
of mosapramine 50 to 300 mg/day in a comparative phase III trial in 159 pat
ients.
Extrapyramidal symptoms (EPS) tended to occur less often and were generally
milder with perospirone than with haloperidol or mosapramine.