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临床试验/EUCTR2009-011470-15-NL
EUCTR2009-011470-15-NL进行中(未招募)1 期

Multicenter, randomized, double-blind, parallel-group extension to study AC 058B201 to investigate the long-term safety, tolerability, and efficacy of 10, 20, and 40 mg/day ponesimod, an oral S1P1 receptor agonist, in patients with relapsing-remitting multiple sclerosis

ACTELION Pharmaceuticals Ltd0 个研究点目标入组 353 人开始时间: 2010年6月3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
353

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

  • 1. Patients who completed study treatment at their regular Week 24 (EOT) visit within the core study (AC-058B201).
  • 2. Signed informed consent for participating in the extension study.
  • 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 353
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • 1. Patients meeting any of the study-specific criteria for permanent discontinuation of study drug, or patients receiving any of the prohibited concomitant medication.
  • 2. Any other clinically relevant medical or surgical condition, which, in the opinion of the investigator, would put the patient at risk by participating in the extension study.

研究者

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