Optimizing a T3 Formulation for COVID-19 Patients With ARDS
- Funded by University of Minnesota
- Total publications:0 publications
Grant number: unknown
Grant search
Key facts
Disease
COVID-19Funder
University of MinnesotaPrincipal Investigator
PhD. Robert SchumacherResearch Location
United States of AmericaLead Research Institution
Center for Translational MedicineResearch Priority Alignment
N/A
Research Category
Clinical characterisation and management
Research Subcategory
Supportive care, processes of care and management
Special Interest Tags
N/A
Study Type
Unspecified
Clinical Trial Details
N/A
Broad Policy Alignment
Pending
Age Group
Not Applicable
Vulnerable Population
Not applicable
Occupations of Interest
Not applicable
Abstract
Some COVID-19 patients are dying from acute respiratory distress syndrome (ARDS), a severe, life-threatening form of respiratory failure characterized by pulmonary edema, inflammation, hypoxemia and a high mortality rate. There are no specific therapies approved for ARDS, and the standard of care is limited to mechanical ventilation, supplemental oxygen and supportive care. Previous research conducted at the University suggests that instillation of triiodothyronine (T3), a naturally-occurring thyroid hormone, directly to the lungs of ARDS patients could increase alveolar fluid clearance, improve oxygenation, and decrease the need for prolonged mechanical ventilation. A clinical formulation of T3 is available but there is no human safety data to support instillation directly into the lungs. The Center for Translational Medicine conducted preclinical studies to demonstrate the safety of direct T3 instillation and enable initiation of a University-sponsored phase I/II clinical trial evaluating the use of T3 for patients with ARDS. Led by Robert Schumacher, PhD, the Center for Translational Medicine's scientific director, researchers in this study will develop a new T3 formulation for the T3-ARDS clinical trial. "Our long-term goal is to develop a safe and effective therapy for patients with ARDS," said Schumacher. "This new formulation will provide a reliable and cost-effective formulation that we can use in the first-in-human T3-ARDS clinical trial."