The effectiveness and safety of amisulpride in Chinese patients with schizophrenia: An 8‐week, prospective, open‐label, multicenter, single‐arm study

نویسندگان

  • Ying Liang
  • Changan Cao
  • Cheng Zhu
  • Chuanyue Wang
  • Congpei Zhang
  • Fang Dong
  • Fude Yang
  • Hong Deng
  • Jingjie Yu
  • Jisheng Tang
  • Lei Su
  • Limin Xin
  • Ling Hong
  • Minglong Gao
  • Muni Tang
  • Shiping Xie
  • Shuiping Lu
  • Tiebang Liu
  • Xiaojin Xu
  • Xijin Wang
  • Xuanzi Li
  • Xueyi Wang
  • Yi Li
  • Yong Zhang
  • Zhiyu Chen
  • Xin Yu
چکیده

INTRODUCTION This study evaluated the effectiveness and safety of amisulpride in Chinese schizophrenia patients. METHODS A multicenter, single-arm Phase IV study (NCT01795183). Chinese patients with schizophrenia received amisulpride for 8 weeks. The primary endpoint was ≥50% decrease in Positive and Negative Syndrome Scale total score from Baseline to Week 8. RESULTS A total of 316 patients were enrolled; 295 were included in the effectiveness analysis; 66.8% (197/295) achieved ≥50% decrease in Positive and Negative Syndrome Scale total score from Baseline to Week 8. Nine patients discontinued treatment because of adverse events. DISCUSSION Amisulpride had clinical effectiveness and was relatively well tolerated in Chinese patients with schizophrenia.

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عنوان ژورنال:

دوره 8  شماره 

صفحات  -

تاریخ انتشار 2016