c19early.org
Ropeginterferon alfa-2b for COVID-19
1 study with 132 patients
Serious outcome risk
Ropeginterferon alfa-2b
Control
Significantly lower risk for ventilation.
COVID-19 Ropeginterferon alfa-2b studies · October 2026
Outcome (studies)
Improvement
Relative risk · 95% CI
All studies (1)−3%
Mortality (1)−3%
RCTs (1)−3%
Early (1)−3%
00.511.5+
← Ropeginterferon
alfa-2b
reduces risk
Increased
risk →
Ropeginterferon Alfa-2b is a long-acting, mono-pegylated recombinant Type I interferon biologic administered via subcutaneous injection.
May 21
2024
Liu et al., Infectious Diseases and Therapy, doi:10.1007/s40121-024-00992-5 A Phase 3, Randomized, Controlled Trial Evaluating the Efficacy and Safety of Ropeginterferon Alfa-2b in Patients with Moderate COVID-19
90% lower ventilation (p=0.04), 3% higher need for oxygen therapy (p=1), and 4% improved recovery (p=1). RCT 132 hospitalized moderate COVID-19 patients in Taiwan showing higher rates of viral clearance or discharge by day 11 with ropeginterferon alfa-2b. The ropeginterferon alfa-2b group also showed higher rates of improvement in lung infil..