NCT07419347

Study of Glecaprevir/Pibrentasvir to Assess Safety Through Real-World Data

Brief summary

The objective of this study is to assess the safety, tolerability and effectiveness of 8-week Glecaprevir/Pibrentasvir (G/P) in participants taking either prescribed or illicit drugs.

Observational study

Status:
Recruiting
Conditions:
Hepatitis C Virus (HCV)
Enrollment:
2000 patients
Protocol ID:
P25-554
Observational model:
Cohort
Time perspective:
Retrospective

 

Eligibility criteria

Participant attributes:
Male and Female

Age:

18 Years and older.

Inclusion Criteria:

- Prescribed 8 weeks of Glecaprevir/Pibrentasvir (G/P).

- Treatment-naïve (for the current infection, participants that may have had prior
infections which were resolved with treatment are considered naive for current
infection as long as they have not received any treatment for the current
infection.)

- Is concomitantly on one or more prescription medications or illicit drugs.

Exclusion Criteria:

- Treated with DAAs other than G/P.

- History of decompensated cirrhosis.

- Had Hepatitis-B virus (HBV) infection.

- Had hepatocellular carcinoma (HCC).

All the cities where the clinical studies are located

Vancouver - V6Z 2C7

British Columbia

Ontario

More information about this study

clinicaltrials.gov