KCT0008637已完成Unknown
Observational study(OS) for efficacy and safety of Fybro® in patients with idiopathic pulmonary fibrosis (IPF)
Yungjin Pharm0 个研究点目标入组 360 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- Unknown
- 状态
- 已完成
- 发起方
- 入组人数
- 360
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
- o Limit 至 o Limit（—）
- 性别
- All
入选标准
- •1. Patients who were diagnosed with idiopathic pulmonary fibrosis, administered Fybro for the first time.
- •2. Signed informed consent form to participate the study.
排除标准
- •1. Those who are contraindicated for administration of this drug according to approval drug information by MFDS
- •1) Patients who are hypersensitive to the main ingredient or additives of this drug
- •2) Patients with severe hepatic impairment or end-stage epilepsy
- •3) Patients with severe renal impairment or end-stage renal disease requiring dialysis
- •4) Patients receiving concomitant fluvoxamine
- •5) Patients with genetic problems such as galactose intolerance, Lapp lactase deficiency or glucose-galactose malabsorption
- •2. A person who uses it for purposes other than approval indication
- •3. Patients who are participating in other clinical trials
研究者
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