跳至主要内容
临床试验/EUCTR2004-002855-15-IT
EUCTR2004-002855-15-IT
进行中(未招募)
不适用

A long term extension to a randomised, double-blind, placebo-controlled, stratified, paralle-group, multicenter, dose-ranging study evaluating four oral doses of TCH346 1.0, 2.5, 7.5 and 15 mg administered once daily in patients with Amyotrophic Lateral Sclerosis

OVARTIS FARMA0 个研究点目标入组 476 人2007年1月8日

概览

阶段
不适用
干预措施
未指定
疾病 / 适应症
Amyotrophic Lateral Sclerosis
发起方
OVARTIS FARMA
入组人数
476
状态
进行中(未招募)
最后更新
14年前

概览

简要总结

暂无简介。

注册库
who.int
开始日期
2007年1月8日
结束日期
待定
最后更新
14年前
研究类型
Interventional clinical trial of medicinal product
性别
All

研究者

发起方
OVARTIS FARMA

入排标准

入选标准

  • 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
  • F.1\.3 Elderly (\>\=65 years) yes
  • F.1\.3\.1 Number of subjects for this age range

排除标准

  • 未提供

结局指标

主要结局

未指定

相似试验

进行中(未招募)
不适用
A long-term extension to a randomized, double-blind, placebo-controlled, stratified, parallel-group, multicenter, dose-ranging study evaluating four oral doses of TCH346 (1.0, 2.5, 7.5 and 15mg) administered once daily in patients with Amyotrophic Lateral Sclerosis.Amyotrophic Lateral Sclerosis
EUCTR2004-002855-15-DEovartis Pharma Services AG480
进行中(未招募)
不适用
A long-term extension to a randomized, double-blind, placebo-controlled, stratified, parallel-group, multicenter, dose-ranging study evaluating four oral doses of TCH346 (1.0, 2.5, 7.5 and 15mg) administered once daily in patients with Amyotrophic Lateral Sclerosis.Amyotrophic Lateral Sclerosis
EUCTR2004-002855-15-GBovartis Pharma Services AG480
进行中(未招募)
3 期
REVEAL 1 (Randomized Evaluation of VGX-3100 and Electroporation for the Treatment of Cervical HSIL)Cervical DysplasiaCervical High Grade Squamous Intraepithelial LesionHSI
TCTR20170301001Inovio Pharmaceuticals, Inc.201
进行中(未招募)
不适用
A LONG-TERM, RANDOMIZED, DOUBLE-BLIND, PARALLEL-GROUP,PLACEBO-CONTROLLED, RADIOGRAPHIC STUDY TO INVESTIGATE THESAFETY AND EFFICACY OF ORALLY ADMINISTERED SD-6010 IN SUBJECTSWITH SYMPTOMATIC OSTEOARTHRITIS OF THE KNEE
EUCTR2007-001457-26-CZPfizer Inc, 235 East 42nd Street, New York, NY 100171,400
进行中(未招募)
不适用
A LONG-TERM, RANDOMIZED, DOUBLE-BLIND, PARALLEL-GROUP, PLACEBO-CONTROLLED, RADIOGRAPHIC STUDY TO INVESTIGATE THE SAFETY AND EFFICACY OF ORALLY ADMINISTERED SD-6010 IN SUBJECTS WITH SYMPTOMATIC OSTEOARTHRITIS OF THE KNEE - ND
EUCTR2007-001457-26-ITPFIZER1,400