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临床试验/NL-OMON35384
NL-OMON35384已完成4 期

Treatment in patients with recurrent infections and IgG Subclass Deficiency, and/or Deficient Anti-Polysaccharide Antibody Response. - Treatment of deficient subclass and/or antipolysaccharide antibody response

Sanquin Plasmaproducten0 个研究点目标入组 60 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
60

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
2 至 99(—)

入选标准

  • IgG subclass deficiency and/or (selective) antipolysaccharide antibody deficiency, and at least 2 physician documented infections before the start of the current treatment or in the last 6 months for newly diagnosed patients.

排除标准

  • - Treatment with any other investigational drug within 7 days prior to study entry, or previous enrolment in this study
  • - Allergic reactions against human plasma/plasma products, or co-trimoxazol
  • - An ongoing progressive terminal disease
  • - Pregnancy or lactation
  • - Renal insufficiency (plasma creatinin > 115 µmol/L; or creatinin clearance <20 ml/min))
  • - An ongoing active disease causing general symptoms e.g. chronic active hepatitis or persistent enterovirus infection with ongoing systemic complaints
  • - Detectable anti-IgA antibodies
  • - Active SLE
  • - Glucose-6-phosphate hydrogenase deficiency

研究者

发起方
Sanquin Plasmaproducten

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