EUCTR2010-020083-38-FR进行中（未招募）1 期
A Multicenter, Study of the Safety of Oseltamivir Administered Intravenously for the Treatment of Influenza in Patients Aged =13 Years
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 入组人数
- 200
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
- •Male and female adults and adolescents, 13 years of age and older
- •Diagnosis of influenza by virology testing or clinical diagnosis based on symptoms suggestive of influenza
- •Less than or equal to 96 hours between the onset of influenza-like illness and first dose of study medication
- •Patient is willing and able to comply with study requirements and give consent, or, if applicable, consent may be given by a parent, legal guardian or legal representative
- •Female patients who are pregnant may be enrolled only if the potential benefit justifies the potential risk to the fetus
- •Female patients who are lactating may be enrolled only if the potential benefit for the lactating mother justifies the potential risk to the breast-fed infant
- •Are the trial subjects under 18? yes
- •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
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Patients with clinical evidence of severe hepatic decompensation at the time of randomization
- •Electrocardiogram showing acute ischemia or significant arrhythmia • Allergy to test medication
- •Patients taking probenicid medication within 7 days before starting study medication
- •Participation in a clinical trial or expanded access trial with an investigational drug in the 4 weeks prior to randomization
研究者
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