drugset / Trial / NCT05185284

Randomized Multicenter Study on the Efficacy and Safety of Favipiravir for Parenteral Administration Compared to Standard of Care in Hospitalized Patients With COVID-19

NCT05185284

Phase 3 Completed 217 enrolled Promomed, LLC Solyur Pharmaceuticals Group · collab
RandomizedParallel-groupOpen-labelTreatment

Summary

This is open-labe randomized multicenter comparative Phase III study conducted in 7 medical facilities. The objective of the study is to assess the efficacy and safety of Favipiravir for parenteral administration compared with the Standard of care (SOC) in hospitalized patients with moderate COVID-19 pneumonia.

Timeline

Start
2021-08-11
Primary completion
2021-12-30
Completion
2021-12-30

Drugs

EvaluationDrugModalityDoseRoute
Comparator Favipiravir Small molecule 800 mg Intravenous
Comparator Remdesivir Small molecule 100 mg

Indications