drugset / Trial / NCT04738136

Safety, Tolerability and Efficacy Of S-1226 in Moderate Severity Covid-19 Bronchiolitis/Pneumonia

NCT04738136

Phase 2 Suspended 30 enrolled SolAeroMed Inc.
RandomizedParallel-groupOpen-labelTreatment

Summary

This is a randomized, open-label, controlled, Phase II proof of concept study to evaluate the safety, tolerability and efficacy of S-1226 in which hospitalized subjects (n≤30) with moderate severity COVID-19 Bronchiolitis/Pneumonia will be enrolled. The safety and tolerability of S-1226 composed of PFOB with ascending doses of carbon dioxide (4%, 8%, and 12% CO2) administered twice daily will be assessed subjects in hospitalized subjects with moderate severity COVID-19 Bronchiolitis/Pneumonia.

Timeline

Start
2021-09-15
Primary completion
2021-10-31
Completion
2021-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Perflubron Other / unclassified 3 ml Inhaled
Subject carbon dioxide Other / unclassified 4 % Inhaled
Subject carbon dioxide Other / unclassified 8 % Inhaled
Subject carbon dioxide Other / unclassified 12 % Inhaled

Indications