Three-Year Outcomes of 6-Month Paliperidone Palmitate in Adults With Schizophrenia

Author:

Correll Christoph U.1234,Johnston Karen5,Turkoz Ibrahim6,Gray Jason5,Sun Liping7,Doring Monica5,Sajatovic Martha8

Affiliation:

1. Department of Psychiatry, Zucker Hillside Hospital, Glen Oaks, New York

2. Department of Psychiatry and Molecular Medicine, Donald and Barbara Zucker School of Medicine at Hofstra/Northwell, Hempstead, New York

3. Department of Child and Adolescent Psychiatry, Charité–Universitätsmedizin Berlin, Berlin, Germany

4. German Center for Mental Health, Berlin, Germany

5. Janssen Scientific Affairs, LLC, a Johnson & Johnson Company, Titusville, New Jersey

6. Janssen Research & Development, LLC, Titusville, New Jersey

7. Cytel, Cambridge, Massachusetts

8. University Hospitals Cleveland Medical Center, Case Western Reserve University School of Medicine, Cleveland, Ohio

Abstract

ImportanceLong-acting injectable (LAI) antipsychotics have the potential to improve adherence and symptom control in patients with schizophrenia, promoting long-term recovery. Paliperidone palmitate (PP) once every 6 months is the first and currently only LAI antipsychotic with an extended dosing interval of 6 months.ObjectiveTo assess long-term outcomes of PP received once every 6 months in adults with schizophrenia.Design, Setting, and ParticipantsIn a 2-year open-label extension (OLE) study of a 1-year randomized clinical trial (RCT), eligible adults with schizophrenia could choose to continue PP every 6 months if they had not experienced relapse after receiving PP once every 3 or 6 months in the 1-year, international, multicenter, double-blind, randomized noninferiority trial. The present analysis focused on patients receiving PP every 6 months in the double-blind trial through the OLE study (November 20, 2017, to May 3, 2022).InterventionPatients received a dorsogluteal injection of PP on day 1 and once every 6 months up to month 30.Main Outcomes and MeasuresEnd points included assessment of relapse and change from the double-blind trial baseline to the OLE end point in Positive and Negative Syndrome Scale (PANSS) total and subscale, Clinical Global Impression–Severity (CGI-S) Scale, and Personal Social Performance (PSP) Scale scores. Treatment-emergent adverse events (TEAEs), injection site evaluations, and laboratory tests were also assessed.ResultsAmong 121 patients (83 [68.6%] male), mean (SD) age at baseline was 38.6 (11.24) years and mean (SD) duration of illness was 11.0 (9.45) years. At screening of the double-blind study, 101 patients (83.5%) were taking an oral antipsychotic and 20 (16.5%) were taking an LAI antipsychotic. Altogether, 5 of 121 patients (4.1%) experienced relapse during the 3-year follow-up; reasons for relapse were psychiatric hospitalization (2 [1.7%]), suicidal or homicidal ideation (2 [1.7%]), and deliberate self-injury (1 [0.8%]). Patients treated with PP every 6 months were clinically and functionally stable, and outcomes were well maintained, evidenced by stable scores on the PANSS (mean [SD] change, −2.6 [9.96] points), CGI-S (mean [SD] change, −0.2 [0.57] points), and PSP (mean [SD] change, 3.1 [9.14] points) scales over the 3-year period. In total, 101 patients (83.5%) completed the 2-year OLE. At least 1 TEAE was reported in 97 of 121 patients (80.2%) overall; no new safety or tolerability concerns were identified.Conclusions and RelevanceIn a 2-year OLE study of a 1-year RCT, results supported favorable long-term outcomes of PP once every 6 months for up to 3 years in adults with schizophrenia.

Publisher

American Medical Association (AMA)

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