EUCTR2019-002283-27-GB进行中(未招募)1 期
A phase 2b, multicenter, randomized, double-blind, placebo-controlled, parallel-group, dose selection study of S-600918 in patients with refractory chronic cough
适应症
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 入组人数
- 372
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •- Having refractory chronic cough (including unexplained chronic cough) for at least 1 year.
- •- If female and of childbearing potential, agreement to use one of the allowed contraceptive methods.
- •- Capable of giving signed informed consent.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 360
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 12
排除标准
- •- Currently smokes or uses potentially irritating inhalational agents (eg, e-cigarettes, smokeless cigarettes, vaping); stopped smoking or using potentially irritating inhalational agents within the last year; or has a smoking history of 20 pack-years or more.
- •- Has chronic obstructive pulmonary disease or uncontrolled asthma.
- •- Has a clinically unstable medical condition.
- •- History of or ongoing significant psychiatric disorder.
- •- History of respiratory tract infection or significant change in lung function or a pulmonary condition in the last 4 weeks.
- •- History of malignancy in the last 5 years.
- •- History of severe drug allergy.
- •- History of alcohol or drug abuse in the last year or currently uses any form of marijuana or illicit drugs.
- •- Has a clinically significant finding on a chest x-ray or chest computed tomography (CT) scan in the last year.
- •- Has systolic blood pressure > 160 mm Hg or diastolic blood pressure > 90 mm Hg.
- •- Received S-600918 previously.
- •- Received an investigational drug in the last 3 months.
- •- Received an angiotensin converting enzyme (ACE) inhibitor in the last 3 months or requires such treatment.
- •- Has a positive serologic test for human immunodeficiency virus (HIV) antigen or antibody, hepatitis B virus surface antigen, or hepatitis C virus ribonucleic acid (RNA).
- •- If female, pregnant or trying to become pregnant or breastfeeding.
研究者
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