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-19
  • Start & end year

    2020
    2020
  • Funder

    Netherlands Organisation for Health Research and Development (ZonMW)
  • Principal Investigator

    Dr. OBJ Corneth
  • Research Location

    N/A
  • Lead Research Institution

    Erasmus MC
  • Research 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.