drugset / Trial / NCT04317040

Efprezimod Alfa (CD24Fc, MK-7110) as a Non-antiviral Immunomodulator in COVID-19 Treatment (MK-7110-007)

NCT04317040 ↗

Phase 3 Completed 234 enrolled Merck & Co., Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study evaluates the efficacy and safety of efprezimod alfa in hospitalized adult participants who are diagnosed with coronavirus disease 2019 (COVID-19) and receiving oxygen support. The primary hypothesis of the study is clinical improvement in the experimental group versus the control group.

Timeline

Start
2020-04-24
Primary completion
2020-10-20
Completion
2020-10-20

Outcome

Met primary endpoint

registry analysis (other test); CD24Fc vs Placebo; p = 0.0367; Hazard Ratio (HR) 1.398 (95% CI 1.020 to 1.918); Log Rank NCT04317040 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject CD24Fc Protein / enzyme biologic 480 mg Intravenous

Indications