跳至主要内容
临床试验/EUCTR2019-001279-34-IT
EUCTR2019-001279-34-IT进行中(未招募)1 期

A multicenter, open-label extension study to evaluate the long-term safety, tolerability and efficacy of orally administered GLPG1690 in subjects with systemic sclerosis -

GALAPAGOS NV0 个研究点目标入组 30 人开始时间: 2021年1月15日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
GALAPAGOS NV
入组人数
30

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

  • - Male or female subjects who completed the 24-week treatment period of Study GLPG1690-CL-204 and who according to the investigator’s judgment may benefit from long-term treatment with GLPG1690.
  • Are the trial subjects under 18? no
  • 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 27
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 3

排除标准

  • - Any condition or circumstances that, in the opinion of the investigator, may make a subject unlikely or unable to complete the study or comply with study procedures and requirements.

研究者

发起方
GALAPAGOS NV

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