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临床试验/NL-OMON50198
NL-OMON50198已完成4 期

Pharmacokinetics of a new paediatric formulation of valacyclovir used for prophylaxis and treatment of VZV and HSV infections in children (VALID II). - VALID-2

Afdeling Apotheek0 个研究点目标入组 7 人开始时间: 待定最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
7

研究概览

简要总结

Trial ended prematurely

研究设计

研究类型
Interventional

入排标准

年龄范围
2 至 11(—)

入选标准

  • 1. Subject is in the age of 1-12 years.
  • 2. Subject receives (val)acyclovir prophylaxis and is planned to receive
  • valacyclovir oral solution.
  • 3. Subject is managed with a central venous catheter (CVC/Port-a-Cath).
  • 4. Subject*s parents have signed the Informed Consent Form prior to screening
  • evaluations.

排除标准

  • 1. Severe anemia (Hb < 5.0 mmol/L).
  • 2. Full dose has not been taken.

研究者

发起方
Afdeling Apotheek

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