Safety and Pharmacokinetics of Micafungin in Children Supported With Extracorporeal Membrane Oxygenation
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 发起方
- 入组人数
- 18
- 试验地点
- 1
- 主要终点
- Pharmacokinetic primary endpoints
研究概览
简要总结
Determine proper dosing of micafungin in children supported with extracorporeal membrane oxygenation (ECMO).
详细描述
Extracorporeal membrane oxygenation (ECMO) is a cardiopulmonary bypass device that provides life-saving, complete respiratory and cardiac support for children who suffer refractory heart or lung failure. While on ECMO, children are at increased risk of infection, including fungal infection. Antifungal prophylaxis can potentially reduce the burden of disease in children on ECMO. Because fungal infections can result in biofilms that are difficult to treat, treatment includes not only antifungal medications but also removal of any large intravenous lines. However, catheter removal for children on ECMO is impossible; therefore, therapy relies upon optimal antifungal management alone.
Micafungin is an antifungal medication that works well against the most common fungal infections and has been shown to be safe in children. Micafungin may be particularly efficacious in children on ECMO because of the drug's ability to penetrate biofilms. However, the ECMO circuit is known to substantially alter drug levels for many drugs, resulting in important dosing changes. Appropriate micafungin dosing in this setting is unknown and sub-optimal dosing might result in therapeutic and prophylactic failure.
Standard dosing of micafungin are 4 and 2 mg per kilogram of body weight given intravenously once daily for treatment and prophylaxis, respectively. Based on preliminary data and modeling from other studies, investigators hypothesize that 8 and 4 mg per kilogram given once daily will achieve proper drug levels to respectively treat and prevent fungal infections in children under 2 years of age who are supported by ECMO. Because the ECMO circuit should have less of an impact on volume of distribution in larger children, investigators hypothesize that in children from 2 to 18 years old, standard dosing of micafungin will achieve proper drug concentrations.
Investigators hold the FDA investigational new drug application (IND #115255) to give micafungin to children on ECMO at the doses described above. Blood samples will be collected at specific times around the first and fourth micafungin doses to describe the pharmacokinetics and drug extraction by the ECMO circuit.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- — 至 18 Years(Child, Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •<= 17.85 years at the time of enrollment.
- •Sufficient venous access to permit administration of study medication.
- •Supported with either venoarterial (VA) or venovenous (VV) ECMO.
- •Availability and willingness of the parent/legal guardian to provide written informed consent.
- •For treatment dosing arm: confirmed or suspected infection
排除标准
- •Subject with a history of anaphylaxis attributed to an echinocandin.
- •Any other concomitant condition, which in the opinion of the investigator would preclude a subject's participation in the study.
- •Previous participation in this study.
- •Pregnancy
研究组 & 干预措施
Treatment Dosing
Age group: 0 - <2y, Micafungin 8 mg/kg/day IV
干预措施: Micafungin (Drug)
Prophylaxis dosing
Age group: 0-<2y, Micafungin 4 mg/kg/day IV
干预措施: Micafungin (Drug)
Standard of care Dosing
Age group: 2-17.85 y, Micafungin standard of care dosing (decided by treating physician)
干预措施: Micafungin (Drug)
结局指标
主要结局
Pharmacokinetic primary endpoints
时间窗: Around the first and fourth doses of micafungin: 0-4h prior to and 0-30 min, 60-90 min, 2-4h, 8-10h, 12-16h, 22-24h after infusion of study drug
Clearance rate (CL), Volume of distribution (V), Oxygenator extraction efficacy
次要结局
- Safety(From Dose 1 until 7 days after the last dose)
研究者
Kevin Watt
Assistant Professor
Duke University
