Drug trial aims to speed recovery from severe COVID lung damage
NCT ID NCT04345614
Summary
This study tested if a new drug called Auxora could help hospitalized adults with severe COVID-19 pneumonia. In the main part of the trial, 284 patients were randomly assigned to receive either Auxora or a placebo (inactive substance) infusion over three days, along with standard care. Researchers measured how long it took patients to recover, aiming to see if Auxora could shorten hospital stays and reduce the need for breathing support.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes NO responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Contacts and locations
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Locations
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Aurora Baycare
Green Bay, Wisconsin, 54311, United States
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Baton Rouge General
Baton Rouge, Louisiana, 70809, United States
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Brigham and Women's Hospital
Boston, Massachusetts, 02115, United States
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Henry Ford Hospital
Detroit, Michigan, 48202, United States
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Houston Methodist Hospital
Houston, Texas, 77030, United States
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John Peter Smith Hospital
Fort Worth, Texas, 76104, United States
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Long Beach Memorial
Long Beach, California, 90806, United States
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Maine Medical Center
Portland, Maine, 04102, United States
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Methodist Hospital
Saint Louis Park, Minnesota, 55426, United States
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National Jewish Health / St. Joseph's Hospital
Denver, Colorado, 80220, United States
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Northwestern University
Chicago, Illinois, 60611, United States
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Regions Hospital
Saint Paul, Minnesota, 55101, United States
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Sharp Memorial San Diego
San Diego, California, 92123, United States
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Sinai Grace
Detroit, Michigan, 48235, United States
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Texas Tech University Medical Center
El Paso, Texas, 79905, United States
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University of Southern California / LA County
Los Angeles, California, 90033, United States
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Virginia Commonwealth University
Richmond, Virginia, 23298, United States
Conditions
Explore the condition pages connected to this study.