drugset / Trial / NCT05808322
Clinical Study for the Efficacy and Safety of Ropeginterferon Alfa-2b in Adult COVID-19 Patients With Comorbidities
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |