EUCTR2022-001837-35-SK进行中(未招募)1 期
A multicenter, open-label, single-arm, multiple-dose study to evaluate the safety, pharmacokinetics, and efficacy of ceftobiprole medocaril in term and pre-term neonates and infants up to 3 months of age with late-onset sepsis
Basilea Pharmaceutica International Ltd, Allschwil0 个研究点目标入组 8 人开始时间: 2022年9月12日最近更新:
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 发起方
- 入组人数
- 8
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
- •1. Informed consent from parent(s) or other legally-acceptable representative (LAR) to participate in the study
- •2. Male or female, with a gestational age of = 24 weeks and a post-natal age ranging from = 3 days to = 3 months
- •3. Diagnosis of documented or presumed bacterial LOS requiring administration of systemic antibiotic treatment.
- •4. Sufficient vascular access to receive study drug and to allow blood sampling at a site separate from the study drug infusion line
- •Are the trial subjects under 18? yes
- •Number of subjects for this age range: 8
- •F.1.2 Adults (18-64 years) no
- •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
- •1. Refractory septic shock not responding to 60 minutes of vasopressor treatment within 48 hours before enrollment
- •2. Proven ventilator-associated pneumonia
- •3. Proven central nervous system infection (e.g., meningitis, brain abscess)
- •4. Proven osteomyelitis, infective endocarditis, or necrotising enterocolitis
- •5. Impaired renal function or known significant renal disease, as evidenced by an estimated glomerular filtration rate (using the Schwartz formula or other applicable formula) calculated to be less than 2/3 of normal for the applicable age group, OR urinary output < 0.5 mL/kg/h (measured over at least 8 hours), OR requirement for dialysis
- •6. Progressively fatal underlying disease, or life expectancy < 30 days
- •7. Use of systemic antibacterial therapy for longer than 72 hours within 7 days before start of study medication
- •8. Participation in another clinical study with an investigational product within 30 days of enrollment in the current study
研究者
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