drugset / Trial / NCT04623021

A Study Evaluating the Efficacy and Safety of CKD-314 (Nafabelltan) in Hospitalized Adult Patients Diagnosed With COVID-19 Pneumonia

NCT04623021 ↗

Phase 2 Completed 104 enrolled Chong Kun Dang Pharmaceutical
RandomizedParallel-groupOpen-labelTreatment

Summary

The primary objective of this study is to evaluate the efficacy of CKD-314 (Nafabelltan) compared to standard of care (SOC), with respect to clinical status assessed by a 7-point ordinal scale in hospitalized adult patients diagnosed with COVID-19 pneumonia

Timeline

Start
2020-09-25
Primary completion
2020-12-12
Completion
2020-12-12

Outcome

Missed primary endpoint

paper There was no significant difference in time to clinical improvement (primary endpoint) between the nafamostat and SOC groups PMID 34723164 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Nafamostat Small molecule 4.8 mg/kg Intravenous

Indications