An Observational Study of Maviret (Glecaprevir/Pibrentasvir) for Korean Chronic Hepatitis C Genotypes 1 to 6 Patients According to the Standard for Re-examination of New Drugs

  • End date
    Sep 30, 2022
  • participants needed
  • sponsor
Updated on 24 January 2021
chronic hepatitis


Post-marketing surveillance study to evaluate the real world safety and effectiveness of Maviret (Glecaprevir/Pibrentasvir) administered under a normal, routine treatment practice by Korean patients with Chronic Hepatitis C Genotypes 1 to 6.


Patients with type C hepatitis genotypes 1-6 who had been prescribed Maviret (glecaprevir/pibrentasvir) in accordance with approved local label. The sample size for this study is due to a requirement by local authorities.

Condition Hepatitis C, Hepatitis C virus
Clinical Study IdentifierNCT03740230
Last Modified on24 January 2021


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Inclusion Criteria

Is your age greater than or equal to 12 yrs?
Gender: Male or Female
Do you have any of these conditions: Hepatitis C virus or Hepatitis C?
Do you have any of these conditions: Hepatitis C or Hepatitis C virus?
Participants with chronic C hepatitis genotypes 1 to 6
Participants prescribed Maviret in accordance with approved local label

Exclusion Criteria

Patients with contraindications to the approved local labels for Maviret
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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