Effectiveness of an arthritis drug in treating a type of severe immune overreaction in patients with COVID-19 induced pneumonia studied.
Effectiveness of an arthritis drug in treating a type of severe immune overreaction in patients with Covid-19 induced pneumonia studied. The clinical trial is enrolling patients at the Harris Health System’s Lyndon B. Johnson Hospital in Houston, Texas.
‘Research has linked a number of Covid-19 deaths to CRS due to damage caused to several major organs.’
The Phase 3 study is evaluating the effectiveness of the drug canakinumab, an interleukin-1 (IL-1) blocker approved for the treatment of juvenile rheumatoid arthritis, for preventing cytokine release syndrome (CRS) in Covid-19 patients with pneumonia. Often referred to as a cytokine storm, CRS is a life-threatening immune reaction caused by the body releasing too many cytokines into the blood at once.
Cytokines include a broad category of proteins secreted by the body.
Interleukin-1 serves as the first-line defence for the immune system, alerting other proteins to respond if a virus or bacteria are present.
Canakinumab blocks the production of IL-1 protein, which could prevent a possible deadly overreaction of the immune system in Covid-19 patients.
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Roberto C. Arduino, MD, the study’s lead investigator and professor of infectious disease at the McGovern Medical School in UTHealth, said this is a time for the HIV research community to utilise the members’ expertise in the search for a treatment for coronavirus.
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"The research community truly feels compelled to do something in the search for a viable treatment for Covid-19, and I feel I owe it to my community to offer my expertise," said Arduino, who has led HIV clinical research for 22 years.
Researchers are investigating if canakinumab combined with standard-of-care treatment can increase the chances of survival without ever requiring invasive mechanical ventilation in patients with Covid-19-induced pneumonia.
Over a two-hour period, patients who are enrolled will receive either a 450 mg, 600 mg, or a 750 mg IV dose of canakinumab based on their body weight, UTHealth said in a statement on Monday. Arduino is the study’s lead investigator.
All participants will be monitored for up to 29 days, or until they are discharged from the hospital. A follow-up will occur at 127 days.
Source-IANS