drugset / Trial / NCT05808322

Clinical Study for the Efficacy and Safety of Ropeginterferon Alfa-2b in Adult COVID-19 Patients With Comorbidities

NCT05808322

Phase 2/3 Unknown 60 enrolled National Taiwan University Hospital
RandomizedParallel-groupOpen-labelTreatment

Summary

To evaluate the efficacy of subcutaneous ropeginterferon alfa 2b ( P1101 combined with standard of care (SOC) compared with standard care alone in adult COVID-19 patients with comorbidities.

Timeline

Start
2023-05-15
Primary completion
2024-05-16
Completion
2024-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Ropeginterferon alfa-2b Protein / enzyme biologic 250 ug Subcutaneous
Subject Ropeginterferon alfa-2b Protein / enzyme biologic 350 ug Subcutaneous
Subject Ropeginterferon alfa-2b Protein / enzyme biologic 500 ug Subcutaneous

Indications