BTK inhibition as therapy for hyper-inflammatory syndrome in COVID-19 patients.
- Funded by Netherlands Organisation for Health Research and Development (ZonMW)
- Total publications:0 publications
Grant number: 1.043E+13
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Key facts
Disease
COVID-19Start & end year
20202020Funder
Netherlands Organisation for Health Research and Development (ZonMW)Principal Investigator
Dr. OBJ CornethResearch Location
N/ALead Research Institution
Erasmus MCResearch Priority Alignment
N/A
Research Category
Therapeutics research, development and implementation
Research Subcategory
Prophylactic use of treatments
Special Interest Tags
N/A
Study Type
Clinical
Clinical Trial Details
Unspecified
Broad Policy Alignment
Pending
Age Group
Unspecified
Vulnerable Population
Unspecified
Occupations of Interest
Unspecified
Abstract
About 5% of all COVID-19 patients become seriously ill and require intensive care. This patient group often develops serious organ damage and has a high risk of death. This is because certain cells of the immune system, especially the monocytes, react too strongly to the virus. This is also called hyper-inflammatory syndrome. The protein Bruton's tyrosine kinase (BTK) is involved, among other things, in monocyte activation and can be inhibited by the specific BTK inhibitor acalabrutinib. Other cells that are very important for killing the virus, such as T cells, are not affected by BTK inhibitors. Research and expected outcome This study will investigate whether treatment with acalabrutinib indeed leads to clinical improvement in hospitalized COVID-19 patients. In addition, the effects of acalabrutinib on the various cells of the immune system are identified in order to gain knowledge about the mechanism of action of acalabrutinib in COVID-19 patients.