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首页> 外文期刊>Schizophrenia research >Paliperidone palmitate maintenance treatment in delaying the time-to-relapse in patients with schizophrenia: A randomized, double-blind, placebo-controlled study
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Paliperidone palmitate maintenance treatment in delaying the time-to-relapse in patients with schizophrenia: A randomized, double-blind, placebo-controlled study

机译:帕潘立酮棕榈酸酯维持治疗可延缓精神分裂症患者的复发时间:一项随机,双盲,安慰剂对照研究

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Objective: We assessed efficacy and tolerability of the injectable atypical antipsychotic paliperidone palmitate in delaying time-to-relapse in adults with schizophrenia.Methods: Eligible patients (Positive and Negative Syndrome Scale [PANSS] total score<120) were transitioned from previous antipsychotics to paliperidone palmitate during a 9-week, open-label phase. Patients received the first 2 intramuscular injections of paliperidone palmitate (50 mg eq) one-week apart, then subsequent injections (25,50, or 100 mg eq, flexibly-dosed), once-monthly. Stable patients (PANSS total score<= 75) continued into the 24-week maintenance phase. At maintenance phase endpoint, stabilized patients were randomized (1:1 ratio) to either continue paliperidone palmitate (at stabilized dose) or begin placebo in the variable-duration, double-blind phase. Results: The preplanned interim analysis (conducted after 68 relapse events) included 312 patients: mean age = 40 years, 55% men, 66% white, and mean transition baseline PANSS total score (SD): placebo, 69.5 (16.89); paliperidone palmitate, 69.3 (17.39). Time-to-relapse (primary endpoint) favored paliperidone palmitate (p<0.0001, log-rank test) at interim and final analysis (n = 408). The hazard ratio (placebo/paliperidone palmitate) at the final analysis was 3.60 (95% CI: 2.45, 5.28). Treatment-emergent adverse event rates (final analysis set) were: 67% for transition and maintenance phases, and 45% (placebo) and 44% (paliperidone palmitate) for the double-blind phase. Across phases, the incidence of glucose-related adverse events was low (<4%), while mean weight increased by 1.9 kg for paliperidone palmitate and remained unchanged for placebo patients. Injection site tolerability was comparable between groups. Conclusion: Paliperidone palmitate significantly delayed time-to-relapse compared with placebo and presented no new safety signals.
机译:目的:我们评估了非典型抗精神病药帕潘立酮棕榈酸酯注射液在延缓精神分裂症成人复发时间中的疗效和耐受性。帕潘立酮棕榈酸酯在9周的开放标签阶段中。患者每隔一周接受两次帕潘立酮棕榈酸酯肌肉注射(50 mg eq),然后每月一次进行后续注射(25,50或100 mg eq,灵活剂量)。稳定的患者(PANSS总分<= 75)继续进入24周维持阶段。在维持阶段终点,将稳定的患者随机(1:1比例)以帕潘立酮棕榈酸酯(稳定剂量)或以可变持续时间,双盲阶段开始安慰剂。结果:预先计划的中期分析(在68次复发事件之后进行)包括312例患者:平均年龄= 40岁,男性55%,白人66%,平均过渡基线PANSS总评分(SD):安慰剂,69.5(16.89);帕潘立酮棕榈酸酯,69.3(17.39)。在中期和最终分析中,复发时间(主要终点)偏爱帕潘立酮棕榈酸酯(p <0.0001,对数秩检验)(n = 408)。最终分析的危险比(安慰剂/帕潘立酮棕榈酸酯)为3.60(95%CI:2.45,5.28)。紧急治疗发生的不良事件发生率(最终分析集)为:过渡和维持阶段为67%,双盲阶段为45%(安慰剂)和44%(帕潘立酮棕榈酸酯)。跨阶段,帕潘立酮棕榈酸酯的葡萄糖相关不良事件发生率低(<4%),而平均体重增加了1.9 kg,而安慰剂患者则保持不变。两组之间的注射部位耐受性相当。结论:与安慰剂相比,帕潘立酮棕榈酸酯显着延迟了复发时间,并且没有新的安全性信号。

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