Authors
Tiziano Prodi, Miriam Olivola, Rodolfo Leuzzi, Monica Biseo, Edoardo Grechi, Nicolaja Girone, Cesare Galimberti, Chiara Di Genova, Kevin La Monica, Federica Calorio, Emma Zuliani, Giada Versaci, Pietro Gallazzi, Norbert Gabriel Kereszteny, Marco Franchini, Andrea Crippa, Gianluca Termine, Roberta Anniverno, Annamaria Cattaneo, Bernardo Dell'Osso
Published in
International clinical psychopharmacology. Jul 22, 2026. Epub Jul 22, 2026.
Abstract
Poor treatment adherence is a major challenge in the management of severe mental disorders, as it is associated with an increased risk of relapse, rehospitalization, symptom worsening, treatment resistance, and all-cause mortality. In 2023 a 2-month 960 mg formulation of aripiprazole 2 months ready-to-use (Ari 2MRTU) was introduced. Compared with monthly long-acting injectable (LAI) drugs, Ari 2MRTU may improve adherence and patient satisfaction by reducing the frequency of healthcare visits. The aim of this prospective longitudinal study was to provide preliminary real-world data on the effectiveness, safety, and acceptability of Ari 2MRTU. Fifty patients, most of whom had previously received aripiprazole, were assessed at baseline, 2 months, and 4 months. Data regarding effectiveness, safety, and acceptability outcomes were collected. Psychometric scores changes were analyzed employing linear mixed-effect regression models accounting for time, age, sex, and previous oral treatment with aripiprazole. Our preliminary findings suggest that Ari 2MRTU is associated with improvements in psychotic symptoms over time, while changes in affective symptoms were less consistent. The findings were also consistent with an overall favorable tolerability profile of Ari 2MRTU. Although adverse events were commonly reported, no unexpected safety signals emerged during the follow-up period, and patients' attitudes toward LAI treatment generally improved over time.
PMID:
42485540
Bibliographic data and abstract were imported from PubMed on 23 Jul 2026.
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