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Study of Intravenous Ampion in Adult COVID-19 Patients Requiring Supplemental Oxygen

COVID-19 Clinical Trial

Official title:
A Randomized, Double-Blinded, Placebo Controlled Phase II Study to Evaluate the Safety and Efficacy of IV Ampion in Adult COVID-19 Patients Requiring Oxygen Supplementation

Clinical Trial Summary

This is a Phase 2 randomized study to evaluate the safety and efficacy of IV Ampion in improving the clinical course and outcomes of adult COVID-19 patients requiring supplemental oxygen.

Clinical Trial Description

Ampion is the low molecular weight filtrate of human serum albumin with the in vitro ability to modulate inflammatory cytokine levels. Ampion has the potential to improve clinical outcomes for COVID-19 patients by reducing inflammatory cytokines correlated with the disease. This study aims to evaluate Ampion and clinical outcomes in patients with COVID-19 requiring supplemental oxygen. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04839965
Study type Interventional
Source Ampio Pharmaceuticals. Inc.
Contact
Status Terminated
Phase Phase 2
Start date July 5, 2021
Completion date April 4, 2022
View Details
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