Glecaprevir/Pibrentasvir Drug Use Results Survey in Patients Infected With Hepatitis C Virus Genotype 1-6
NCT ID: NCT03341871
Last Updated: 2021-09-20
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
1095 participants
OBSERVATIONAL
2017-12-27
2020-09-15
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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HCV Genotypes 1, 2, 3, 4, 5, or 6 participants
Participants receiving combination therapy with the glecaprevir plus pibrentasvir (GLE/PIB) regimen according to the current local label.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
0 Years
99 Years
ALL
No
Sponsors
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AbbVie
INDUSTRY
Responsible Party
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Principal Investigators
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AbbVie Inc.
Role: STUDY_DIRECTOR
AbbVie
Locations
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Abbvie Japan /ID# 161985
Tokyo, , Japan
Countries
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Related Links
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clinical study report synopsis
Other Identifiers
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P16-570
Identifier Type: -
Identifier Source: org_study_id
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