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临床试验/JPRN-jRCT2080221423
JPRN-jRCT2080221423未知3 期

Phase III study of KW-2246 (A double blind study of KW-2246 compared to placebo for breakthrough pain episodes in cancer patients)

Kyowa Hakko Kirin Co., Ltd.0 个研究点开始时间: 2011年3月30日最近更新:

试验速览

阶段
3 期
发起方

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
>= 20age old 至 ot applicable(—)
性别
All

入选标准

  • Written informed consent
  • - Have been treated with opioid analgesic on a fixed-schedule at a stable daily dose
  • - Receiving at least 1 but not more than 4 doses of rescue medication per day in average and whose pain is controlled
  • - ECOG PS =< 3

排除标准

  • - Currently suffered from intolerable opioid-specific adverse reactions due to opioid analgesics
  • - Ssevere respiratory dysfunction
  • - Severe bradyarrhythmia
  • - Severe hepatic function disorder
  • - Severe renal function disorder
  • - Severe psychoneurotic disorder
  • - Susceptibility to respiratory depression due to such conditions as increased intracranial pressure, head injury or brain tumor

研究者

发起方
Kyowa Hakko Kirin Co., Ltd.

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