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Published on: June 20, 2020
Sofosbuvir and Ribavirin Therapy for Children Aged 3 to <12 Years With Hepatitis C Virus Genotype 2 or 3 Infection
Philip Rosenthal1, Kathleen B Schwarz2, Regino P Gonzalez-Peralta3
1University of California San Francisco, San Francisco, CA.
Insights
Sofosbuvir plus ribavirin offers a highly effective and well-tolerated treatment for children with chronic hepatitis C virus (HCV) genotypes 2 or 3. This combination therapy achieved a 98% sustained virologic response rate in young patients.
Area of Science:
- Hepatology
- Pediatric Infectious Diseases
- Virology
Background:
- Current hepatitis C virus (HCV) treatment for children under 12 years is limited to pegylated interferon plus ribavirin.
- Limited treatment options necessitate evaluation of newer antiviral therapies for pediatric HCV.
- HCV infection in children can lead to long-term liver complications if untreated.
Purpose of the Study:
- To evaluate the safety and efficacy of sofosbuvir plus ribavirin in children aged 3 to <12 years with chronic HCV genotypes 2 or 3.
- To determine appropriate dosing of sofosbuvir and ribavirin in different age and weight groups within the pediatric population.
- To assess the sustained virologic response rate 12 weeks after therapy (SVR12) as the primary efficacy endpoint.
Main Methods:
- An open-label study involving 54 children (3 to <12 years) with chronic HCV genotypes 2 or 3.
- Sofosbuvir dosing varied by age and weight (150 mg or 200 mg daily).
- Ribavirin dosing was weight-based (up to 1,400 mg/day in two divided doses).
Main Results:
- A high SVR12 rate of 98% (53/54 patients) was achieved.
- The most common adverse events were vomiting, headache, and diarrhea.
- One serious adverse event involved accidental ribavirin overdose in a 3-year-old, who recovered and completed treatment.
Conclusions:
- Sofosbuvir plus ribavirin is a well-tolerated and highly effective treatment for chronic HCV genotypes 2 or 3 in children aged 3 to <12 years.
- The study confirms the appropriateness of the selected sofosbuvir doses through pharmacokinetic sampling.
- This regimen represents a significant advancement over existing treatments for pediatric HCV.
Abstract:
Currently, the only approved hepatitis C virus (HCV) treatment for children aged <12 years is pegylated interferon plus ribavirin. In an open-label study, we evaluated the safety and efficacy of sofosbuvir plus ribavirin for 12 weeks in children aged 3 to <12 years chronically infected with genotype 2 or for 24 weeks in patients with genotype 3. Patients aged 3 to <6 years weighing <17 kg received sofosbuvir 150 mg, and patients aged 3 to <6 years weighing ≥17 kg and all patients aged 6 to <12 years received sofosbuvir 200 mg once daily. Intensive pharmacokinetic sampling conducted in each age group confirmed the appropriateness of sofosbuvir doses. For all patients, ribavirin dosing was determined by baseline weight (up to 1,400 mg/day, two divided doses). The primary efficacy endpoint was sustained virologic response 12 weeks after therapy (SVR12). Fifty-four patients were enrolled (41 aged 6 to <12 years and 13 aged 3 to <6 years). Most were treatment naïve (98%) and infected perinatally (94%). All but one patient achieved SVR12 (53/54, 98%; 95% confidence interval, 90%-100%). The patient who did not achieve SVR12 was a 4-year-old who discontinued treatment after 3 days because of "abnormal drug taste." The most commonly reported adverse events in patients aged 6 to <12 years were vomiting (32%) and headache (29%), and those in patients aged 3 to <6 years were vomiting (46%) and diarrhea (39%). One 3-year-old patient had a serious adverse event of accidental ribavirin overdose requiring hospitalization for monitoring; this patient completed treatment and achieved SVR12. Conclusion: Sofosbuvir plus ribavirin was well tolerated and highly effective in children aged 3 to <12 years with chronic HCV genotype 2 or 3 infection.
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