An Observational Study of Peginterferon (e.g. Pegasys)-Based Direct Acting Antiviral Triple Therapy in Patients With Chronic Hepatitis C Genotype 1
| Status: | Completed |
|---|---|
| Conditions: | Hepatitis |
| Therapuetic Areas: | Immunology / Infectious Diseases |
| Healthy: | No |
| Age Range: | 18 - Any |
| Updated: | 4/21/2016 |
| Start Date: | January 2012 |
| End Date: | March 2014 |
Non-Interventional, Prospective Cohort Study of the Effectiveness, Safety and Utilization of Two Approved Pegylated Interferon-Based Direct Acting Antiviral Triple Therapies in the Management of Genotype 1 Chronic Hepatitis C in Routine Clinical Practice in the USA
This prospective observational study will evaluate the efficacy and safety of two approved
pegylated interferon-based direct acting antiviral triple therapies in patients with chronic
hepatitis C genotype 1. Patients receiving pegylated interferon (e.g. Pegasys) and ribavirin
plus either telaprevir or boceprivir in accordance with local standard of care and US
labeling will be followed for the duration of their treatment and for up to 24 weeks
post-treatment.
pegylated interferon-based direct acting antiviral triple therapies in patients with chronic
hepatitis C genotype 1. Patients receiving pegylated interferon (e.g. Pegasys) and ribavirin
plus either telaprevir or boceprivir in accordance with local standard of care and US
labeling will be followed for the duration of their treatment and for up to 24 weeks
post-treatment.
Inclusion Criteria:
- Adult patients, >/= 18 years of age
- Chronic hepatitis C, genotype 1
- Receiving pegylated interferon-based direct acting antiviral therapy (pegylated
interferon and ribavirin plus either telaprevir or boceprivir) in accordance with
local standard of care and US labeling
Exclusion Criteria:
- Contraindications per US labels
We found this trial at
66
sites
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