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Published on: September 27, 2018
[Real data o viral hepatitis C therapy in the Czech Republic]
Insights
This study shows 100% efficacy for interferon-free therapy in Czech Republic chronic hepatitis C patients using paritaprevir/ritonavir, ombitasvir, and dasabuvir. The treatment achieved sustained virological response (SVR12) in all participants.
Area of Science:
- Hepatology
- Virology
- Pharmacology
Background:
- Chronic hepatitis C remains a significant global health concern.
- Interferon-free therapies have revolutionized hepatitis C treatment.
- Real-world data on novel treatment regimens are crucial for clinical practice.
Purpose of the Study:
- To evaluate the efficacy of an interferon-free regimen for chronic hepatitis C in the Czech Republic.
- To assess the sustained virological response (SVR12) in a diverse patient population.
- To report the first real-world data on this specific combination therapy.
Main Methods:
- A cohort of 109 chronic hepatitis C patients were treated.
- The regimen included paritaprevir/ritonavir, ombitasvir, and dasabuvir, with or without ribavirin.
- Patients included treatment-naive and treatment-experienced individuals, predominantly infected with genotype 1b.
Main Results:
- A 100% sustained virological response 12 weeks after therapy termination (SVR12) was achieved.
- This high efficacy was observed across treatment-naive and treatment-experienced groups.
- No virological treatment failures were reported in the analyzed cohort.
Conclusions:
- The combination therapy of paritaprevir/ritonavir, ombitasvir, and dasabuvir is highly effective for chronic hepatitis C.
- This interferon-free regimen offers a promising treatment option in the Czech Republic.
- Real-world data confirm the excellent outcomes of this direct-acting antiviral therapy.
Abstract:
We reported the first real data about efficacy of interferon-free therapy of chronic hepatitis C in the Czech Republic. Patients were treated with combined therapy of paritaprevir/ritonavir + ombitasvir + dasabuvir with or without ribavirin. There were 109 patients, predominantly men - 62 (57 %), most of them infected by genotype 1b - 101 patients (93 %), minority infected by genotypes 1a (6/109, 5 %) and 4 (2/109, 2 %). Both treatment-naive (43/109, 39 %), and treatment-experienced patients (66/109, 61 %) were treated. Sustained virological response 12 weeks after therapy termination (SVR12) was 100 %, with exclusion of patients with other reason than virological treatment failure.Key words: dasabuvir - chronic hepatitis C - ombitasvir - paritaprevir/rinonavir - ribavirin.

