Johnson & Johnson Pharmaceutical Research and Development, LLC, Raritan, NJ 08560, USA.
J Clin Psychopharmacol. 2010 Jun;30(3):235-44. doi: 10.1097/JCP.0b013e3181dd3103.
This study assessed the efficacy and the safety of a dosing regimen that was revised from earlier studies for the investigational injectable atypical antipsychotic paliperidone palmitate (approved in the USA, August 2009) for adult patients with acutely exacerbated schizophrenia. The patients (N = 652) were randomly assigned (1:1:1:1) to paliperidone palmitate at 25, 100, or 150 mg eq. or placebo in this 13-week double-blind study. The patients received an injection of paliperidone palmitate at 150 mg eq. or placebo in the deltoid muscle on day 1 and the assigned fixed dose or placebo in the deltoid or gluteal [corrected] on day 8 and then once monthly (days 36 and 64). No oral supplementation was used. Target plasma levels were achieved by day 8 in all paliperidone palmitate groups. The mean change in Positive and Negative Syndrome Scale total score from baseline to end point improved significantly (P < or = 0.034) in all the paliperidone palmitate dose-groups versus placebo. Paliperidone palmitate treatment with this revised dosing regimen led to the achievement of rapid and consistent therapeutically effective plasma levels that were maintained by once-monthly dosing in either the deltoid or gluteal muscle. Common treatment-emergent adverse events (> or =2% of patients in any of the treatment groups) that occurred more frequently in the total paliperidone palmitate group versus the placebo group (with > or =1% difference) were injection-site pain (7.6% vs 3.7%), dizziness (2.5% vs 1.2%), sedation (2.3% vs 0.6%), pain in the extremity (1.6% vs 0.0%), and myalgia (1.0% vs 0.0%). The paliperidone palmitate treatment was efficacious and generally tolerated across the dose range (25, 100, or 150 mg eq.) in adult patients with acutely exacerbated schizophrenia.
这项研究评估了一种剂量方案的疗效和安全性,该方案是对先前研究中用于治疗急性加重精神分裂症成年患者的研究性注射用非典型抗精神病药棕榈酸帕利哌酮(于 2009 年 8 月在美国获批)进行修订后的方案。共有 652 名患者被随机(1:1:1:1)分配至棕榈酸帕利哌酮 25、100 或 150mg eq. 或安慰剂组,进行为期 13 周的双盲研究。患者在第 1 天接受一次肌肉注射 150mg eq. 剂量的棕榈酸帕利哌酮或安慰剂,然后在第 8 天接受一次肩胛或臀肌注射固定剂量的药物或安慰剂,之后每月一次(第 36 天和第 64 天)。未使用口服补充剂。所有棕榈酸帕利哌酮组均在第 8 天达到目标血浆浓度。与安慰剂组相比,所有棕榈酸帕利哌酮剂量组的阳性和阴性症状量表总分从基线到终点的平均变化均显著改善(P < 或 = 0.034)。采用修订后的剂量方案进行棕榈酸帕利哌酮治疗可快速且持续地达到有效的治疗性血浆水平,每月一次肩胛或臀肌注射可维持该水平。在所有治疗组中发生率均大于 2%(任何治疗组中发生率大于 1%)的常见治疗后出现的不良反应有注射部位疼痛(7.6%比 3.7%)、头晕(2.5%比 1.2%)、镇静(2.3%比 0.6%)、肢体疼痛(1.6%比 0.0%)和肌痛(1.0%比 0.0%)。在急性加重精神分裂症成年患者中,棕榈酸帕利哌酮在 25、100 或 150mg eq. 剂量范围内具有疗效,且总体耐受性良好。