HOST RESPONSE MEDIATORS IN CORONAVIRUS (COVID-19) INFECTION - IS THERE A PROTECTIVE EFFECT OF ARBs ON OUTCOMES OF CORONAVIRUS INFECTION? (ARBs CORONA II)

  • Funded by Canadian Institutes of Health Research (CIHR)
  • Total publications:0 publications

Grant number: 172629

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Key facts

  • Disease

    COVID-19
  • Start & end year

    2020
    2020
  • Known Financial Commitments (USD)

    $2,626,971.16
  • Funder

    Canadian Institutes of Health Research (CIHR)
  • Principal Investigator

    Pending
  • Research Location

    Canada
  • Lead Research Institution

    University of British Columbia Medicine
  • Research Priority Alignment

    N/A
  • Research Category

    Therapeutics research, development and implementation

  • Research Subcategory

    Prophylactic use of treatments

  • Special Interest Tags

    N/A

  • Study Subject

    Clinical

  • Clinical Trial Details

    Randomized Controlled Trial

  • Broad Policy Alignment

    Pending

  • Age Group

    Unspecified

  • Vulnerable Population

    Unspecified

  • Occupations of Interest

    Unspecified

Abstract

As the COVID-19 pandemic continues to spread globally, the World Health Organization (WHO) and others are actively conducting clinical trials for anti-virals to combat this disease. However, many of the severe complications of COVID-19 are caused by the host's response to viral infection. We have a unique opportunity to complement these ongoing studies with our clinical trial to test how modulating the host response can improve outcomes for hospitalized COVID-19 patients. We plan to re-purpose a class of drugs called angiotensin II receptor blockers (ARBs), which are normally used to treat high blood pressure and other cardiovascular diseases. ARBs have been shown to prevent lung injury in influenza (the flu), which is caused by a virus that uses similar mechanisms as SARS-CoV-2 (the virus that causes COVID-19) to enter human cells. We will recruit 1,732 patients from multiple sites throughout Canada and randomize them to be treated with either Losartan (a commonly prescribed ARB with an excellent safety profile), or to continue under usual care. We will evaluate whether patients who receive Losartan have better outcomes, such as decreased mortality and organ dysfunction, than those who receive usual care. At the same time, we will collect blood samples from these patients to determine whether there are certain molecular "markers" that can predict mortality and their response to Losartan. This study will provide guidance on whether Losartan can be used to limit organ dysfunction and mortality in hospitalized COVID-19 patients, ultimately resulting in better care and outcomes for patients during this global pandemic.