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[Ledipasvir/sofosbuvir combination for chronic hepatitis C infection in children and adolescents]
Jesús Quintero1, Javier Juampérez1, Ecaterina Julio1
1Unidad de Hepatología y Trasplante hepático pediátrico, Hospital Universitari Vall d'Hebron, Universitat Autònoma de Barcelona, Barcelona, España.
Insights
Ledipasvir/sofosbuvir combination therapy is safe and effective for treating chronic Hepatitis C Virus (HCV) genotypes 1 and 4 in children. All pediatric patients achieved a sustained virologic response, demonstrating treatment efficacy.
Area of Science:
- Hepatology
- Virology
- Pediatric Infectious Diseases
Background:
- Hepatitis C virus (HCV) infection poses a significant global health challenge.
- Chronic HCV infection in pediatric populations requires effective and safe treatment options.
Purpose of the Study:
- To evaluate the safety and efficacy of the ledipasvir/sofosbuvir combination for treating chronic HCV genotypes 1 and 4 in pediatric patients.
- To assess sustained virologic response 12 weeks post-treatment (SVR12) in this cohort.
Main Methods:
- A cohort of pediatric patients aged 6 to 18 years with chronic HCV genotypes 1 or 4 received ledipasvir/sofosbuvir.
- Treatment duration and dosage were individualized based on age, fibrosis stage, and prior treatment history.
- The primary endpoint was the percentage of patients achieving SVR12.
Main Results:
- Nine pediatric patients (median age 14.8 years) were treated; 8 had fibrosis, and 5 had prior treatment experience.
- HCV RNA became undetectable in 100% of patients by 6 weeks, with all achieving SVR12.
- Adverse effects were mild, including headache and oral thrush in 33.3% of patients.
Conclusions:
- Ledipasvir/sofosbuvir is a safe and effective treatment for pediatric patients with chronic HCV genotypes 1 and 4.
- The observed SVR12 rates are comparable to those reported in adult populations.
Introduction:
Hepatitis C virus infection is world health problem. The aim of this study was to assess the safety and efficacy of ledipasvir/sofosbuvir combination in chronic Hepatitis C Virus (HCV) genotype 1 and 4 infection in paediatric patients.
Methods:
Eligible patients to be treated with ledipasvir/sofosbuvir were patients from 6 to 18 years old with a chronic HCV genotype 1 or 4 infection. The duration and doses of antiviral drugs were changed depending on patient age, fibrosis stage, and PEGylated interferon+ribavirin experience status. The primary efficacy endpoint was the percentage of patients with a sustained virological response 12 weeks post-treatment.
Results:
A total of nine patients (7 males) with a median age of 14.8 years (8.48-17.91) were treated with ledipasvir/sofosbuvir combination. Five patients received previous treatment with PEGylated interferon+ribavirin during a median of 8.5 months (3-12 months). Eight patients had some degree of fibrosis (1 patient presented with F1, three patients F2, 2 patients F3, and 2 patients F4). The median pre-treatment viral load was 6.2 Log [5.9-6.8] with the HCV RNA becoming negative six weeks after starting the treatment in 100% of the patients. All patients maintained a sustained viral response at 12 weeks. Three patients (33.3%) had some type of adverse effect (2 headache and one oral thrush). The median post-treatment follow-up was 24 weeks (12-104).
Conclusions:
Treatment with ledipasvir/sofosbuvir in paediatric patients with chronic HCV infection genotype 1 and 4 is safe and effective with SVR12 and similar to those reported in adults.
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