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临床试验/EUCTR2004-000283-27-GB
EUCTR2004-000283-27-GB进行中(未招募)1 期

A Pilot Open-Label Study to Investigate the Safety and Anti-inflammatory Effects of VX-765, an Orally Administered Interleukin-1ß Converting Enzyme Inhibitor, in Patients with Muckle-Wells Syndrome

Vertex Pharmaceuticals Incorporated0 个研究点目标入组 6 人开始时间: 2005年2月14日最近更新:

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
6

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

  • Confirmed diagnosis of Muckle-Wells syndrome, as defined by mutations of the NALP3/CIAS1 gene, associated with laboratory evidence of acute phase response; symptoms of rash, conjunctivitis, fever, fatigue, or arthralgia; SAA greater than 10 mg/L on 2 consecutive occasions, patient agreement to discontinue anti-inflammatory medications.
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Pregnancy/lactation, any chronic inflammatory disorder other than Muckle-Wells Syndrome, medication that may alter drug absorption, recent use of other investigational drugs, recent blood/plasma donation, drug allergy/hypersensitivity

研究者

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