跳至主要内容
临床试验/JPRN-jRCT2080220563
JPRN-jRCT2080220563未知3 期

Randomized, Placebo-controlled, Double-blind, Parallel-group, Confirmatory Study of SM-13496 (lurasidone HCl) in Patients with Schizophrenia <Phase III Study>

Sumitomo Dainippon Pharma Co., Ltd.0 个研究点目标入组 460 人开始时间: 2008年6月9日最近更新:
适应症

试验速览

阶段
3 期
入组人数
460

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 18age old 至 <= 74age old(—)
性别
All

入选标准

  • - Patient meets DSM-IV criteria for schizophrenia.
  • - Patient is 18 or older but younger than 75 years of age on the day of signing informed consent.
  • - Patient understands the objectives, nature, and other aspects of the study and voluntarily agrees to participate in the study by providing written informed consent.

排除标准

  • - Patient has a history of neuroleptic malignant syndrome, water intoxication, or paralytic ileus.
  • - Patient has Parkinson's disease.
  • - Patient has a history or complication of malignancy.

研究者

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