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临床试验/EUCTR2014-004911-35-Outside-EU/EEA
EUCTR2014-004911-35-Outside-EU/EEA进行中(未招募)不适用

A Multicenter, Open-Label, Noncomparative Study to Evaluate the Safety, Tolerability, and Efficacy of Caspofungin Acetate in Children with Documented Candida or Aspergillus Infections - Documented Candida or Aspergillus Infections in Pediatric Patients

Merck & Co., Inc.0 个研究点目标入组 50 人开始时间: 2015年4月3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)
入组人数
50

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

  • The patient is at least 3 months of age and younger than 18 years of age at time of study drug administration.
  • Clinical evidence of infection must be present at some time within 48 hours prior to enrollment.
  • Inclusion Criteria for Patients With Aspergillus Infections: 1) Patients must meet definitions of proven or probable invasive aspergillosis (as specified in criteria developed by the European Organization for Research and Treatment of Cancer/Invasive Fungal Infections Co- Operative Group (EORTC/IFICG) and the National Institute of Allergy and Infectious Diseases - Mycoses Study Group (NIAID-MSG)
  • Inclusion Criteria for Patients With Esophageal Candida Infections, Patients with a diagnosis of esophageal candidiasis based on symptoms, endoscopy and microbiology or histopathology for whom IV therapy is appropriate.
  • Inclusion Criteria for Patients With Invasive Candida Infections, Patient must have at least 1 positive culture of a Candida species from blood or other normally sterile body site, which has been obtained within 4 days of study entry.
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range: 49
  • 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

  • Patient is <3 months or =18 years of age (at time of the first dose of study drug administration).
  • Patient has any of the following abnormal laboratory values: a) International normalization ratio (INR) >1.6 or, if patient is receiving anticoagulants, INR >4.0. b) Bilirubin >3 times the upper limit of normal for age. c) AST (SGOT) or ALT (SGPT) >5 times the upper limit of normal for age. d) Platelet count <5000/µL.

研究者

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