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临床试验/JPRN-jRCT1080222732
JPRN-jRCT1080222732未知Unknown

Specific post-marketing surveillance of pazufloxacin (Pasil) Clinical efficacy and safety of pazufloxacin administered at a dose of 1,000 mg twice daily

Toyama Chemical Co., Ltd.(Current FUJIFILM Toyama Chemical Co., Ltd.)0 个研究点目标入组 300 人开始时间: 2015年1月29日最近更新:

试验速览

阶段
Unknown
发起方
入组人数
300

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
ot applicable 至 ot applicable(—)
性别
All

入选标准

  • 1. Target disease: sepsis, severe or intractable respiratory tract infections (pneumonia, secondary infection of chronic respiratory diseases), or the pneumonia caused by Streptococcus pneumoniae
  • 2. Age: 15 years of age and older
  • 3. Gender : Both
  • 4. Patients administered at a dose of 1,000 mg twice daily

排除标准

  • 1. Patients in whom drug efficacy of pazufloxacin (Pasil) was difficult to assess

研究者

发起方
Toyama Chemical Co., Ltd.(Current FUJIFILM Toyama Chemical Co., Ltd.)

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