Table 7.
Overview of the clinical efficacy of dopamine receptor partial agonists (DRPA).
| • All DRPAs have evidence of acute antipsychotic efficacy that is comparable: it is lower than in some other AP2G (clozapine, amisulpride, olanzapine, and risperidone) |
| • All DRPAs have comparable evidence of preventing relapse of schizophrenia |
| • Aripiprazole (≥15 mg/day) and cariprazine (≥3 mg/day) are effective in acute mania |
| • Cariprazine (1.5–3 mg/day) is effective in bipolar depression |
| • Aripiprazole in monotherapy (15–30 mg/day), as addon (10–30 mg/day), or LAI (400 mg/4 weeks) is effective in maintenance treatment of bipolar disorder and for preventing relapse to mania |
| • Aripiprazole (5–15 mg/day) and brexpiprazole (≥2 mg/day) are effective as adjunctive treatment for major depression with insufficient response |
| • Cariprazine (4.5 mg/day) is effective in treatment of primary, predominant negative symptoms of schizophrenia |
| • Aripiprazole i.m. injection (9.75 mg/day) is effective for acute agitation in psychosis or bipolar disorder |
| • Brexpiprazole (2 mg/day) has potential efficacy in the management of acute agitation in Alzheimer's dementia |
| • Aripiprazole has evidence of efficacy in other indications: treatment of schizophrenia and bipolar disorder in children and adolescents (10–17 years), clozapine augmentation in refractory schizophrenia, adjunctive treatment of obsessive–compulsive disorder (OCD), tic disorders, and autism spectrum disorders |