NL-OMON39678已完成3 期
MAGNITUDE-A Phase 3 Evaluation of the Safety and Efficacy of Lambda/RBV/DCV in Treatment Naïve Subjects with Chronic HCV Infection, who have Underlying Mild or Moderate Hemophilia or Patients who are Prior Relapsers to Pegylated interferon alfa/RBV;Revised Protocol 01 Incorporates Amendment 02 and Administrative Letter 01 and 02;+ Pharmacogenetics Blood Sample Amendment Number 01 - Site Specific (version 1.0, dated 11-Sep-12) - AI452-030
Bristol-Myers Squibb0 个研究点目标入组 10 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
- 入组人数
- 10
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
- 18 至 99（—）
入选标准
- •Infection with the hepatitis C virus (HCV) with underlying mild or moderate hemophilia;• Males 18 years of age and above ;• Have not been previously treated with an interferon
排除标准
- •Not infected with the hepatitis C virus (HCV), hepatitis D virus (HDV) or human immunodeficiency virus (HIV);• Do not have a serious liver, psychiatric, blood, thyroid, lung, heart or eye disease;• Presence of Bethesda inhibitor
研究者
相似试验
进行中（未招募）
不适用
A Phase 3 Evaluation of the Safety and Efficacy of Lambda/RBV/DCV in Treatment Naïve Subjects with Chronic HCV Infection, who have Underlying Mild or Moderate Hemophilia or Patients who are Prior Relapsers to Pegylated interferon alfa/RBVChronic Hepatitis C Virus Infection (Genotype 1b, 2, 3, 4)MedDRA version: 14.1Level: PTClassification code 10008912Term: Chronic hepatitis CSystem Organ Class: 10021881 - Infections and infestationsEUCTR2012-003463-22-NLBristol-Myers Squibb International Corporation130
进行中（未招募）
1 期
A Phase 3 Evaluation of the Safety and Efficacy of Lambda/RBV/DCV inTreatment Naïve Subjects with Chronic HCV Infection, who haveUnderlying Mild or Moderate Hemophilia or Patients who are PriorRelapsers to Pegylated interferon alfa/RBVChronic Hepatitis C Virus Infection(Genotype 1b, 2, 3, 4)MedDRA version: 14.1Level: PTClassification code 10008912Term: Chronic hepatitis CSystem Organ Class: 10021881 - Infections and infestationsEUCTR2012-003463-22-ITBRISTOL-MYERS SQUIBB INTERNATIONAL CORPORATIO130
进行中（未招募）
不适用
A Phase 3 Evaluation of the Safety and Efficacy of Lambda/RBV/DCV in Treatment Naïve Subjects with Chronic HCV Infection, who have Underlying Mild or Moderate Hemophilia or Patients who are Prior Relapsers to Pegylated interferon alfa/RBVEUCTR2012-003463-22-ESBristol-Myers Squibb International Corporation130
进行中（未招募）
1 期
Safety and efficacy study in subjects with chronic HCV and underlying hemophiliaChronic Hepatitis C Virus Infection (Genotype 1b, 2, 3, 4)MedDRA version: 17.0Level: PTClassification code 10008912Term: Chronic hepatitis CSystem Organ Class: 10021881 - Infections and infestationsEUCTR2012-003463-22-ROBristol-Myers Squibb International Corporation71
进行中（未招募）
1 期
Rollover Study to Evaluate the Safety and Efficacy of Long-term Treatment with Lumacaftor in Combination with Ivacaftor.MedDRA version: 20.0Level: PTClassification code 10011762Term: Cystic fibrosisSystem Organ Class: 10010331 - Congenital, familial and genetic disordersCystic FibrosisEUCTR2015-001644-11-SEVertex Pharmaceuticals Incorporated256