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临床试验/JPRN-jRCT2080222672
JPRN-jRCT2080222672未知2 期

A Phase II, multi-center, randomized, double-blind study of T-4288 in patients with community-acquired pneumonia

Toyama Chemical Co., Ltd.(Current FUJIFILM Toyama Chemical Co., Ltd.)0 个研究点开始时间: 2014年11月27日最近更新:
适应症

试验速览

阶段
2 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

  • 1. Age: 20 years of age and older
  • 2. Gender : Both
  • 3. Confirmed clear infiltrative shadow by chest X-ray or CT within 48 hours prior to the first administration of the study drug
  • 4. Confirmed at least one of the following changes in laboratory values;
  • -WBC increased (WBC > 10000 /mm3)
  • -Stab cell > 15%
  • -WBC decreased (WBC < 4500 /mm3)
  • 5. Confirmed at least one of the following clinical symptoms and/or findings:
  • -Abnormal findings on auscultation and/or percussion
  • -Dyspnea or tachypnea
  • -Hypoxemia

排除标准

  • 1. Having improvement of clinical symptoms due to pneumonia by other systemic antibiotics
  • 2. Having a history of allergy to macrolide or quinolone antibiotics

研究者

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

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