Effect of Lurasidone on Life Engagement in Schizophrenia: Post-Hoc Analysis of the JEWEL Study.

antipsychotic agents efficacy life engagement lurasidone schizophrenia

Journal

Neuropsychiatric disease and treatment
ISSN: 1176-6328
Titre abrégé: Neuropsychiatr Dis Treat
Pays: New Zealand
ID NLM: 101240304

Informations de publication

Date de publication:
2024
Historique:
received: 29 02 2024
accepted: 03 07 2024
medline: 29 7 2024
pubmed: 29 7 2024
entrez: 29 7 2024
Statut: epublish

Résumé

To evaluate the effect of lurasidone on a new, patient Life Engagement scale in schizophrenia. This post-hoc analysis included participants (ages 18 to 74) diagnosed with schizophrenia who were randomized to lurasidone (40 mg/day) or placebo in a 6-week double-blind efficacy study and those who continued in a subsequent 12-week open-label extension study during which patients received either 40 or 80/mg day lurasidone (flexibly dosed). Change in life engagement was measured using the Positive and Negative Syndrome Scale (PANSS) 11-item Life Engagement subscale score, and individual subscale items, at week 6 during the double-blind phase and extension phase week 12 during the open-label extension phase. Analysis focused on 478 subjects randomized to lurasidone or placebo during the 6-week trial, and 146 who received lurasidone during the extension phase. During the 6-week trial, there was a significantly greater change on the PANSS This post-hoc analysis suggests that lurasidone may improve life engagement in patients with schizophrenia, a meaningful outcome from patients' perspective. Further studies are needed to confirm this effect. Trial registration: EudraCT Numbers: 2016-000060-42; 2016-000061-23.

Identifiants

pubmed: 39072313
doi: 10.2147/NDT.S466479
pii: 466479
pmc: PMC11283796
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1453-1463

Informations de copyright

© 2024 Maruyama et al.

Déclaration de conflit d'intérêts

I Miura reports personal fees from Sumitomo Pharma Co., Ltd., Eisai, Janssen, Meiji Seika Pharma, MSD, Otsuka, Takeda, Tanabe-Mitsubishi, Towa, Yoshitomi, Viatris, outside the submitted work. H Maruyama, F Sano, R Sakaguchi, and K Okamoto are full-time employees of Sumitomo Pharma Co., Ltd. The authors report no other conflicts of interest in this work.

Auteurs

Hidenori Maruyama (H)

Medical Science, Sumitomo Pharma Co., Ltd, Osaka, Japan.

Fumiya Sano (F)

Department of Data Science, Drug Development Division, Sumitomo Pharma Co., Ltd, Tokyo, Japan.

Reiko Sakaguchi (R)

Department of Clinical Research, Drug Development Division, Sumitomo Pharma Co., Ltd, Tokyo, Japan.

Keisuke Okamoto (K)

Department of Clinical Operation, Drug Development Division, Sumitomo Pharma Co., Ltd, Tokyo, Japan.

Itaru Miura (I)

Department of Neuropsychiatry, Fukushima Medical University, Fukushima, Japan.

Classifications MeSH