跳至主要内容
临床试验/CTRI/2013/02/003428
CTRI/2013/02/003428已完成未知

Association of IL-28 Single Nucleotide Polymorphisms with SVR Rates in HCV Patients within the Asia-Pacific Region

MSD PHARMACEUTICALS PVT LTD0 个研究点目标入组 1,330 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
1,330

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

入选标准

  • (1)Patients of Asian ethnicity.
  • (2)Patients diagnosed with chronic HCV genotype 1 (only).
  • (3)Patients initiated on PegIFN-α and ribavirin combination therapy with the last dose completed 6 months prior to and treated within the last 5 years from the date of centre initiation.
  • (4)Patients naïve to previous PegIFN-α and ribavirin combination therapy.
  • (5)Patients willing to provide consent and a blood sample for IL-28B analysis.
  • (6)Patients aged 18 years and above.

排除标准

  • (1)Co-infected HCV patients (HBV and HIV).
  • (2)Active intravenous drug users at the start of combination therapy.
  • (3)Known chronic alcoholic at the start of combination therapy (in the judgement of the physician).
  • (4)Patients with decompensated liver disease or other causes of liver disease (such as autoimmune hepatitis) at the start of combination therapy.
  • (5)Patients suffering from chronic renal failure.
  • (6)Patients suffering from thalassemia.
  • (7)Patients that have undergone a liver transplantation before or during the PegIFN+ribavirin treatment course.
  • (8)Patients with evidence of hepatocellular carcinoma at the start of combination therapy.
  • ((9)Patients of mixed ethnicity (e.g. White Caucasian and Asian mix, etc.).
  • (10)Patients who are currently pregnant.

研究者

发起方
MSD PHARMACEUTICALS PVT LTD

相似试验

Study to evaluate association of genetic marker... | 临床试验