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临床试验/EUCTR2022-001837-35-SK
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

发起方
Basilea Pharmaceutica International Ltd, Allschwil

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