RPCEC00000418尚未招募1 期
Safety evaluation and preliminary effect of the monoclonal antibody Nimotuzumab in the treatment of patients with acute respiratory distress syndrome (ARDS)
Center of Molecular Immunology (CIM)0 个研究点目标入组 74 人开始时间: 2023年3月3日最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 74
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized controlled trial. Masking: Open. Control group: Active. Assignment: Parallel. Purpose: Treatment
入排标准
- 年龄范围
- 19 years 至 none（—）
- 性别
- All
入选标准
- •1. Mild or moderate ARDS, with subpulmonary or extrapulmonary phenotype.
- •2. Any gender and skin color
- •3. Age equal to or greater than 19 years
- •4. Patients with signed informed consent
排除标准
- •1 Pregnancy or breastfeeding.
- •2. History of known HIV, hepatitis B or C infection (referred by the patient or their representative).
- •3 Known allergy or hypersensitivity to any component of the formulation under study.
- •4. Minimal probability of survival and a life expectancy of less than 3-5 days as defined by an APACHE II score of = 35 at enrollment.
- •5 Be receiving another investigational product.
研究者
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