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OpenTrials
Completed

NCT Number: NCT01453244

Pharmacogenomic Research in Korean Patients With Hepatitis C

The aim of this study is to investigate the relationships between drug response and the host genetic factors, viral factors and clinical factors in chronic hepatitis C patients (HCV). And thus, the investigators are trying to develop the pharmacogenomic guideline in the Korean patients with HCV.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Hepatitis C virus infected patients

Exclusion criteria

  • Patients who infected Hepatitis B virus or Human immunodeficiency virus
  • HCV infected patients previously treated with antiviral drugs
  • Patients had a history of autoimmune hemolytic anemia

Treatment and study plan

Primary outcomes

  1. Sustained virological response (SVR)

    Time frame: 24 weeks after the end of treatment

    Undetectable HCV RNA in serum ( <15 IU/ml ) 24 weeks after the end of treatment

Secondary outcomes

  1. Anemia

    Time frame: 4 weeks after start of treatment

    • a reduction in Hemoglobin of >3.0 g/dL
    • a reduction in Hemoglobin levels to 10.0g/dL.

Sponsors and collaborators

Lead sponsor

Inje University

Other

Registry information

Official study title

Pharmacogenomic Research for Prediction of Drug Response in Korean Patients With Hepatitis C

Important dates

Study start
2011
Primary completion
2013
Study completion
2013
First posted
Oct 17, 2011
Registry last updated
Jun 3, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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