EUCTR2006-004432-70-IT进行中（未招募）不适用
A multicenter phase II study to evaluate the safety, tolerability and efficacy of caspofungin as prophylactic treatment of invasive fungal infections in patients with acute leukemia undergoing induction chemotherapy - ProFIL-C
AZIENDA OSPEDALIERA SPEDALI CIVILI DI BRESCIA0 个研究点开始时间: 2006年11月10日最近更新:
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
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
- •- all patients with a diagnosis af acute leukemia who are enrolled in the clinical protocols of NILG for acute leukemia at diagnosis - age 18 - written 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
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •- presence of clinical, radiological or microbiological evidence of invasive fungal infection at enrollment - concomitant use of systemic parenteral or oral antifungal agents - hypersensitivity, or any serious reaction to echinocandin - pregnancy or breast-feeding - acute hepatitis or moderate/severe hepatic insufficiency of any cause; - recent prior use of caspofungin - concomitant use of rifampin, carbamazepine, phenytoin, fenobarbital, or other inducers of CYP450 enzymes
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