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Öğe FLEXIBLY DOSED PALIPERIDONE PALMITATE IN NON-ACUTE PATIENTS WITH SCHIZOPHRENIA SWITCHED FROM PREVIOUSLY UNSUCCESSFUL MONOTHERAPY WITH ORAL ATYPICAL ANTIPSYCHOTICS(Elsevier Science Bv, 2014) Hargarter, Ludger; Bergmans, Paul; Cherubin, Pierre; Rancans, Elmars; Bez, Yasin; Parellada, Eduardo; Carpiniello, Bernado[Abstract Not Available]Öğe Intramuscular long-acting paliperidone palmitate in acute patients with schizophrenia unsuccessfully treated with oral antipsychotics(Pergamon-Elsevier Science Ltd, 2015) Hargarter, Ludger; Cherubin, Pierre; Bergmans, Paul; Keim, Sofia; Rancans, Elmars; Bez, Yasin; Parellad, EduardIn this prospective multicentre, open-label, 6-month study (Paliperidone Palmitate Flexible Dosing in Schizophrenia [PALMFlexS]), tolerability, safety and treatment response with paliperidone palmitate (PP) were explored in patients with acute symptoms of schizophrenia following switching from previously unsuccessful treatment with oral antipsychotics. This pragmatic study was conducted in a large, more representative sample of the general schizophrenia population compared to randomized controlled pivotal trials, to specifically mimic real-world clinical situations. After initiation on Day 1 and Day 8, patients received PP once monthly at flexible doses (50-150mg eq.) intramuscularly. The primary efficacy outcome was defined as the percentage of patients achieving >= 30% improvement in PANSS total score from baseline (BL) to last-observation-carried-forward (LOCF) endpoint (EP). Safety and tolerability assessments included Extrapyramidal Symptom Rating Scale (ESRS) total score and treatment-emergent adverse events (TEAEs). Overall, 212 patients received PP at least once after switching from oral antipsychotics, primarily due to lack of efficacy (45.8%). Significant improvements from BL in mean (SD) PANSS total score were observed from Day 8 onwards (BL to LOCF EP: - 31.0 [29.0]; p < 0.0001). At endpoint, two-thirds (66.7%) and 43.5% of patients achieved a >= 30% and >= 50% improvement in mean PANSS total score, respectively. PP was associated with significant improvements across secondary measures of symptom severity, subjective well-being, medication satisfaction, illness-related disorders of activity and participation, and patient functioning (p < 0.0001; BL to LOCF EP). PP was generally well tolerated, with significant reductions in ESRS total score (p < 0.0001) and mainly mild-to-moderate TEAEs. TEAEs reported in >= 5% of patients were injection-site pain (13.7%), insomnia (10.8%), psychotic disorder (10.4%), headache and anxiety (both 6.1%). The PALMFlexS study findings provide valuable pragmatic clinical data on PP treatment in patients with acute schizophrenia previously unsuccessfully treated with oral antipsychotics. (C) 2014 The Authors. Published by Elsevier Inc.Öğe ONCE MONTHLY PALIPERIDONE PALMITATE - TOLERABILITY AND TREATMENT RESPONSE IN RECENTLY DIAGNOSED VERSUS CHRONIC NON-ACUTE SCHIZOPHRENIA PATIENTS SWITCHED FROM PREVIOUSLY UNSUCCESSFUL TREATMENT WITH ORAL ANTIPSYCHOTICS(Elsevier Science Bv, 2014) Hargarter, Ludger; Bergmans, Paul; Cherubin, Pierre; Rancans, Elmars; Bez, Yasin; Parellada, Eduardo; Carpiniello, Bernardo[Abstract Not Available]Öğe PALIPERIDONE PALMITATE - IMPACT ON NEGATIVE, DISORGANIZED AND DEPRESSIVE SYMPTOMS, SUBJECTIVE WELL-BEING AND PATIENT SATISFACTION IN PATIENTS WITH SCHIZOPHRENIA PREVIOUSLY UNSUCCESSFULLY TREATED WITH ORAL ANTIPSYCHOTICS(Elsevier Science Bv, 2014) Schreiner, Andreas; Hargarter, Ludger; Bergmans, Paul; Cherubin, Pierre; Rancans, Elmars; Bez, Yasin; Parellada, Eduardo[Abstract Not Available]
