Evidence map›Paper›PMID 42102150›Full record

ArticleThe international journal of neuropsychopharmacology2026

Life engagement improvements with cariprazine in schizophrenia: a post-hoc analysis of PANSS data from short-term studies.

Réka Csehi, Péter Szabó, Zsófia Borbála Dombi, Thomas Brevig, Balázs Szatmári, Ágota Barabássy

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Article in The international journal of neuropsychopharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Réka CsehiGlobal Medical Division, Gedeon Richter Plc., Budapest, Hungary.ORCID 0000-0001-5485-363X
Péter SzabóGlobal Medical Division, Gedeon Richter Plc., Budapest, Hungary.
Zsófia Borbála DombiGlobal Medical Division, Gedeon Richter Plc., Budapest, Hungary.ORCID 0000-0002-0390-4852
Thomas BrevigGlobal Medical Division, Gedeon Richter Plc., Budapest, Hungary.
Balázs SzatmáriGlobal Medical Division, Gedeon Richter Plc., Budapest, Hungary.
Ágota BarabássyGlobal Medical Division, Gedeon Richter Plc., Budapest, Hungary.

Funding

Gedeon Richter Plc.
6 · The paper itself

Abstract

objectivePatient life engagement (PLE) is increasingly recognized as a meaningful treatment goal in schizophrenia, yet it remains under-researched, partly due to the lack of validated PLE measures. This post-hoc analysis evaluated the effect of cariprazine on PLE using a 14-item subset of the Positive and Negative Syndrome Scale (PANSS).

methodsData from three 6-week, randomized, double-blind, placebo-controlled trials were pooled and analyzed post-hoc. The 14-item PANSS subset measured PLE across four domains: Cognitive, Social, Emotional, and Physical. Changes from baseline to Week 6 in PLE Total Score and domain scores were analyzed using mixed models for repeated measures. Responder rates (≥5- and ≥ 10-point reductions) were further assessed.

resultsCariprazine (n = 880; 1.5-6.0 mg/day) showed significantly greater improvements than placebo (n = 446) on PLE Total Score (LS mean difference [LSMD] = -3.23; 95% CI: -4.59 to -1.87; Cohen's d = 0.79, P < .001) and across Emotional (LSMD: -0.59; 95% CI: -0.97 to -0.22; Cohen's d = 0.49, P < .001), Social (LSMD: -1.13; 95% CI: -1.65 to -0.6; Cohen's d = 0.71, P < .001), and Cognitive (LSMD: -1.34; 95% CI: -1.91 to -0.76; Cohen's d = 0.77, P < .001) domains, and numerically greater improvement on the Physical (LSMD: -0.25; 95% CI: -0.5 to 0.01; Cohen's d = 0.30, P = .071) domain. Statistically significant improvements emerged by Week 2 on the PLE Total and were sustained through Week 6. Responder analyses showed that 81% and 57% of cariprazine-treated patients met the ≥5- and ≥ 10-point thresholds, respectively, versus 64% and 43% with placebo (both P < .001).

conclusionThe results suggest that cariprazine is associated with significant improvements in patient life engagement in schizophrenia based on the 14-item subset of the PANSS, with early and clinically meaningful benefits across domains. These findings support the value of cariprazine in addressing patient-centered treatment goals. Significant outcomes Cariprazine produced significantly greater overall symptom and illness-severity improvements than placebo, with large effect sizes on both PANSS Total (LSMD -7.44) and CGI-S (LSMD -0.41). Cariprazine showed consistently superior reductions in PLE Total and domain scores - especially Social, Cognitive, and Emotional domains - and demonstrated significantly faster and larger weekly improvements from Week 2 onward in PLE Total. Clinically meaningful response rates were higher with cariprazine, with 81% achieving ≥5-point improvement and 57% achieving ≥10-point improvement, both significantly outperforming placebo. Limitations As a post-hoc analysis, it is inherently exploratory and subject to limitations of the original study designs. While recently validated through a robust process, this 14-item subset of the PANSS is a new tool. Its performance over longer time periods, ability to predict functional outcomes, and usefulness across diverse clinical populations still need further investigation. Finally, the studies could not control for external psychosocial factors that may influence life engagement, like participation in psychosocial interventions, caregiver support or follow-up with mental health professionals.

Indexed as

Antipsychotic AgentsOutcome Assessment, Health CarePiperazinesSchizophreniaSchizophrenic PsychologyAdultDouble-Blind MethodFemaleHumansMaleMiddle AgedPsychiatric Status Rating ScalesRandomized Controlled Trials as TopicTreatment OutcomeAntipsychotic AgentscariprazinePiperazinescariprazinelife engagementpartial agonistschizophrenia

Identifiers

PMID42102150
PMCPMC13220802

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.