drugset / Trial / NCT04389671

The Safety and Preliminary Tolerability of Lyophilized Lucinactant in Adults With Coronavirus Disease 2019 (COVID-19)

NCT04389671

Phase 2 Completed 20 enrolled Windtree Therapeutics
NaSingle-groupOpen-labelTreatment

Summary

This is a multicenter, single-treatment study. Subjects will consist of adults with COVID-19 associated acute lung injury who are being cared for in a critical care environment.

Timeline

Start
2021-01-05
Primary completion
2022-02-20
Completion
2022-02-20

Drugs

EvaluationDrugModalityDoseRoute
Subject Lucinactant Peptide 80 mg/kg