Condition: Acute Respiratory Distress Syndrome · Coronavirus · Hypoxic Respiratory Failure · Sponsor: PhaseBio Pharmaceuticals Inc.
This is a multicenter, randomized, double-blind, parallel group study to investigate the efficacy of pemziviptadil (PB1046) by improving the clinical outcomes in hospitalized COVID-19 patients at high risk for rapid clinical deterioration, acute respiratory distress syndrome (ARDS) and death. The study will enroll approximately 210 hospitalized COVID-19 patients who require urgent decision-making and treatment at approximately 20 centers in the United States.
This description comes directly from the study's public registry record.
No contact information is available for this study as per the public registry record.
Always discuss trial participation with your own doctor first.
| Baptist Health Research Institute | Jacksonville, Florida, United States | — |
| Sarasota Memorial Hospital | Sarasota, Florida, United States | — |
| The University of Kansas Medical Center | Kansas City, Kansas, United States | — |
| Adventist Healthcare White Oak Medical Center | Silver Spring, Maryland, United States | — |
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