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A Study of the Effectiveness of Peginterferon Alfa-2a (Pegasys) and Ribavirin Treatment in Slovenian Hepatitis C (HCV) Patients

Roche logo

Roche

Status

Completed

Conditions

Hepatitis C, Chronic

Treatments

Drug: Peginterferon alfa-2a
Drug: Ribavirin

Study type

Observational

Funder types

Industry

Identifiers

NCT02556307
ML22263

Details and patient eligibility

About

In this Slovenian, multi-center, observational study, the effectiveness of standard of care Peginterferon alfa-2a + ribavirin treatment in adult patients with chronic hepatitis C (CHC) is examined. Patients were treated for 24- or 48-weeks, as prescribed by the treating physician, followed by a 24-week follow-up period.

Enrollment

270 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Male and female patients >/= 18 years
  • Positive test for HCV
  • Effective contraception as specified by the Peginterferon alfa-2a and/or ribavirin labels

Exclusion criteria

  • Concomitant infection with HIV or hepatitis B
  • Participation in a clinical trial within 30 days prior to study start
  • Any contraindications specified in the Peginterferon alfa-2a and ribavirin product labels

Trial design

270 participants in 1 patient group

Peginterferon alfa-2a + Ribavirin
Treatment:
Drug: Ribavirin
Drug: Peginterferon alfa-2a

Trial contacts and locations

4

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Data sourced from clinicaltrials.gov

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