Efficacy and safety of aripiprazole once-monthly in Asian patients with schizophrenia: A multicenter, randomized, double-blind, non-inferiority study versus oral aripiprazole

被引:59
作者
Ishigooka, Jun [1 ]
Nakamura, Jun [2 ]
Fujii, Yasuo [3 ]
Iwata, Nakao [4 ]
Kishimoto, Toshifumi [5 ]
Iyo, Masaomi [6 ]
Uchimura, Naohisa [7 ]
Nishimura, Ryoji [8 ]
Shimizu, Naoaki [9 ]
机构
[1] Tokyo Womens Med Univ, Dept Psychiat, Shinjuku Ku, Tokyo 1628666, Japan
[2] Univ Occupat & Environm Hlth, Sch Med, Dept Psychiat, Yahata Nishi Ku, Kitakyushu, Fukuoka 8078555, Japan
[3] Yamanashi Prefectural Kita Hosp, Dept Neuropsychiat, Nirasakishi, Yamanashi 4070046, Japan
[4] Fujita Hlth Univ, Dept Psychiat, Sch Med, Toyoake, Aichi 4701192, Japan
[5] Nara Med Univ, Dept Psychiat, Sch Med, Kashihara, Nara 6348521, Japan
[6] Chiba Univ, Dept Psychiat, Sch Med, Chuou Ku, Chiba 2608670, Japan
[7] Kurume Univ, Dept Neuropsychiat, Sch Med, Kurume, Fukuoka 8300011, Japan
[8] Fukuoka Univ, Dept Psychiat, Fac Med, Jonan Ku, Fukuoka 8140180, Japan
[9] Otsuka Pharmaceut Co Ltd, Minato Ku, Tokyo 1088242, Japan
关键词
Aripiprazole; Long-acting injection; Schizophrenia; Asian; Efficacy; Safety; MAINTENANCE TREATMENT; PLACEBO; RELAPSE; ANTIPSYCHOTICS; SCALE; DEPOT; TERM;
D O I
10.1016/j.schres.2014.12.013
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Objective: This study was designed to evaluate efficacy and safety of aripiprazole once-monthly (AOM) by verifying non-inferiority of AOM to oral aripiprazole in Asian patients with schizophrenia. Method: The study consisted of a screening phase and three phases: an oral conversion phase (<= 12 weeks), an oral stabilization phase (<= 12 weeks) and a 52-week double-blind phase. Patients meeting stabilization criteria for 4 weeks during the oral stabilization phase were randomly assigned (1: 1) to AOM (400 mg) or oral aripiprazole (6-24 mg/day). The primary endpoint was Kaplan-Meier estimated rate of non-exacerbation of psychotic symptoms/non-relapse at Week 26. Results: A total of 724 patients were screened, and 502 patients entered the oral stabilization phase. Of 455 patients randomized in the double-blind phase, 228 received AOM and 227 received oral aripiprazole. The non-exacerbation of psychotic symptoms/non-relapse rates at Week 26 were 95.0% (AOM) and 94.7% (oral aripiprazole) and the difference was 0.3% (95% CI: -3.9,4.5), thus non-inferiority of AOM compared to oral aripiprazole with respect to non-exacerbation of psychotic symptoms/non-relapse rate was shown with a margin of -3.9% which is well above the pre-defined non-inferiority limit (-15%). The proportions of patients meeting exacerbation of psychotic symptoms/relapse criteria and stabilization of psychotic symptoms/maintenance criteria were 6.6% and 92.5% in both groups. Discontinuation rates due to all reasons were 25.9% (AOM) and 33.5% (oral aripiprazole). AOM was well tolerated as well as oral aripiprazole. Conclusions: Non-inferiority of AOM to oral aripiprazole was established. AOM is efficacious in maintenance treatment of stabilized schizophrenia, with comparable efficacy and tolerability to oral aripiprazole. Clinical Trials Registration: JapicCTI-101175 (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:421 / 428
页数:8
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