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Monotherapy treatment with cariprazine for the treatment of predominant negative symptoms of patients with schizophrenia: A double-blind, active comparator-controlled trial

Published online by Cambridge University Press:  23 March 2020

G. Németh*
Affiliation:
Gedeon Richter Plc, medical division, Budapest, Hungary
M. Debelle
Affiliation:
Gedeon Richter Plc, medical division, Budapest, Hungary
I. Laszlovszky
Affiliation:
Gedeon Richter Plc, medical division, Budapest, Hungary
E. Szalai
Affiliation:
Gedeon Richter Plc, medical division, Budapest, Hungary
B. Szatmári
Affiliation:
Gedeon Richter Plc, medical division, Budapest, Hungary
J. Harsányi
Affiliation:
Gedeon Richter Plc, medical division, Budapest, Hungary
Á. Barabássy
Affiliation:
Gedeon Richter Plc, medical division, Budapest, Hungary
S. Durgam
Affiliation:
Forest research institute, clinical development, Jersey City, USA
I. Bitter
Affiliation:
Semmelweis university, department of psychiatry and psychotherapy, Budapest, Hungary
S. Galderisi
Affiliation:
University of Naples SAN, psychiatry, Naples, Italy
*
*Corresponding author.

Abstract

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Objective

To examine the effect of cariprazine, a dopamine D3/D2 receptor partial agonist with preferential binding to D3 receptors, on predominant negative symptoms of schizophrenia.

Methods

Subjects with schizophrenia and PANSS factor score for negative symptoms (PANSS-FSNS) ≥ 24 and no pseudospecific factors (e.g. extrapyramidal symptoms, depression) were randomized to cariprazine 4.5 mg/d (dose range: 3-6 mg/d) or risperidone 4 mg/d (dose range: 3-6 mg/d) for 6 months.

Results

Four hundred and sixty-one patients were randomized 1:1 to double-blind risperidone (n = 231) or cariprazine (n = 230) treatment. Change from Baseline (CfB) at week 26 in the primary parameter, PANSS-FSNS, was larger in the cariprazine group than in the risperidone group (LSMD = −1.47; 95% CI: [−2.39, −0.53]; P = 0.002) significant from week 14 onwards. CfB at week 26 in the functional parameter, Personal and Social Performance (PSP) total score, showed similarly greater improvement with cariprazine than risperidone (LSMD = 4.63; 95% CI: [2.71, 6.56]; P < 0.001) significant from week 10 onward. Statistically significant differences in favor of cariprazine at week 26 were shown in the PSP areas of self-care, socially useful activities and personal and social relationships. Most patients tolerated the study treatment well, as reflected by low discontinuation rates due to adverse events (AEs). Adverse event profiles of cariprazine and risperidone were similar. The most common AEs during study treatment were insomnia (10.0%), and headache (10.4%), both in the risperidone group.

Conclusion

26-week cariprazine treatment, given as antipsychotic monotherapy, was significantly more effective on negative symptoms and on functioning than risperidone in patients with predominant negative symptoms of schizophrenia.

Disclosure of interest

The authors have not supplied their declaration of competing interest.

Type
EW534
Copyright
Copyright © European Psychiatric Association 2014
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