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Paliperidone extended-release in patients with non-acute schizophrenia previously unsuccessfully treated with other
Andreas Schreiner1, Marjolein Lahaye, Joseph Peuskens
1Medical & Scientific Affairs Europe, Middle East & Africa, Janssen-Cilag GmbH , Johnson & Johnson Platz 5a, 41470 Neuss , Germany +49 2137 955 153 ; +49 2137 955 92 5481 ; aschrein@its.jnj.com.
Objective:
This study explores relevant outcomes with flexibly dosed paliperidone extended-release (ER) in a real-world design.
Research Design And Methods:
Patients were recruited from 23 countries. Adults with non-acute schizophrenia (n = 1812), previously unsuccessfully treated with other oral antipsychotics, were transitioned to paliperidone ER and prospectively treated for 6 months.
Main Outcome Measures:
Primary efficacy outcome for patients switching for the main reason of lack of efficacy was ≥ 20% improvement in Positive and Negative Syndrome Scale (PANSS) total scores. For patients switching for main reasons other than lack of efficacy, primary outcome was non-inferiority in efficacy compared with the previous medication.
Results:
Among the lack-of-efficacy group, 61% achieved a ≥ 20% improvement in PANSS total scores from baseline to endpoint. For switchers from other than the lack-of-efficacy group, efficacy maintenance after switching to paliperidone ER was confirmed. Clinically relevant and statistically significant symptomatic improvements occurred for each patient group based on main reason for switching.
Conclusion:
Paliperidone ER was well tolerated and associated with a meaningful clinical response in patients who switched from other oral antipsychotics, with insomnia and anxiety as most frequent side-effects.
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