drugset / Trial / NCT04494984

A Study to Investigate the Pharmacokinetics, Efficacy and Safety of INM005 in Patients With COVID-19.

NCT04494984 ↗

Phase 2/3 Completed 243 enrolled Inmunova S.A.
RandomizedSequentialQuadruple-blindTreatment

Summary

This study aims to analyze the efficacy and safety of passive immunotherapy by administering an equine hyperimmune serum (INM005) against the SARS-CoV-2 receptor binding domain (RBD) to COVID-19 patients. Improvement of the clinical course 28 days after the start of treatment will be evaluated.

Timeline

Start
2020-07-27
Primary completion
2020-11-23
Completion
2020-12-30

Drugs

EvaluationDrugModalityDoseRoute
Comparator INM005 Unknown 4 mg/kg Intravenous

Indications