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A double-stranded DNA virus of the Orthopoxvirus family, mpox (formerly monkeypox), continues to infect people daily, following the 2022 global outbreak.1 Two clades (clade 1 and clade 2) have been identified, with the 2022 outbreak caused by a subclade of clade 2, referred to as clade 2b.2 Comparatively, clade 1 leads to a more severe disease state and greater […]

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Angela Haczku: I-SPY COVID-19 – Cyclosporine in critically ill patients with COVID-19

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Published Online: Sep 14th 2022

I-SPY COVID-19 (NCT04488081) is a phase 2, multi-centre, open-label, platform clinical trial designed by Quantum Leap Healthcare Collaborative™ to rapidly evaluate repurposed and investigational agents in critically ill patients infected with SARS-CoV-2. In this interview, we speak with Prof. Angela Haczku (University of California at Davis, CA, USA), one of the study investigators for the cyclosporine arm of the study. Cyclosporine is a frequently prescribed immunosuppressant that was hypothesized to be of potential benefit in critically ill patients with COVID-19 due to its possible ability to suppress the ‘cytokine storm’ and hence reduce the chance of COVID-19-related lung injury. However, the testing of cyclosporine in I-SPY COVID-19 was recently discontinued when the drug failed to meet the pre-defined primary outcome criteria. In this interview, we discuss the trial and its results in more detail.

Questions:

  1. What is the rationale for the use of cyclosporine in patients hospitalized with COVID-19? (0:17)
  2. What were the aims and design of the I-SPY COVID trial? (0:58)
  3. Why was the cyclosporine arm terminated? (3:05)
  4. What factors might have contributed to this disappointing finding, and what questions remain unanswered? (4:14)
  5. What are the future goals for the I-SPY study? (6:36)

Disclosures: Angela Haczku has nothing to disclose in relation to this video interview.

Support: Interview and filming supported by Touch Medical Media. Interview conducted by Katey Gabrysch.

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