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CompletedNCT03303599

Study of the Effectiveness and Clinical Practice Use of Glecaprevir Plus Pibrentasvir in Patients With Chronic Hepatitis C Genotypes 1 to 6

Real World Evidence of the Effectiveness and Clinical Practice Use of Glecaprevir Plus Pibrentasvir in Patients With Chronic Hepatitis C Genotypes 1 to 6

Status
Completed
Phase
Study type
Observational
Enrollment
2,118 (actual)
Sponsor
AbbVie · Industry
Sex
All
Age
Healthy volunteers
Not accepted

Summary

The interferon- and ribavirin- (RBV) free combination regimen of glecaprevir plus pibrentasvir (GLE/PIB) for the treatment of genotypes 1 to 6 of chronic hepatitis C (CHC) viral infection has been shown to be safe and effective in randomized controlled clinical trials. This observational study is an effectiveness research examining the regimen of GLE/PIB, used according to local label, under real world conditions in a clinical practice patient population.

Conditions

Timeline

Start date
2017-11-13
Primary completion
2020-01-24
Completion
2020-01-24
First posted
2017-10-06
Last updated
2021-05-19

Locations

156 sites across 9 countries: Austria, Belgium, France, Greece, Israel, Italy, Poland, Portugal, Switzerland

Source: ClinicalTrials.gov record NCT03303599. Inclusion in this directory is not an endorsement.

Study of the Effectiveness and Clinical Practice Use of Glecaprevir Plus Pibrentasvir in Patients With Chronic Hepatitis (NCT03303599) · Clinical Trials Directory