4.6 Review

Janus Kinase Inhibitors and Coronavirus Disease (COVID)-19: Rationale, Clinical Evidence and Safety Issues

Journal

PHARMACEUTICALS
Volume 14, Issue 8, Pages -

Publisher

MDPI
DOI: 10.3390/ph14080738

Keywords

coronavirus disease (COVID)-19; janus kinase (JAK) inhibitors; baricitinib; ruxolitinib; real word evidence; adverse effects; drug interaction

Funding

  1. Institutional Research Funds (Ricerca Fondamentale Orientata)

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There is a paradigm shift in drug development and clinical practice to combat COVID-19, with a focus on testing various pharmacological approaches like JAK inhibitors. These inhibitors possess key characteristics for successful repurposing, including convenient oral administration, favorable pharmacokinetic profiles, and dual anti-inflammatory and anti-viral effects. Efforts are also being made to address safety issues and expand usage in different patient populations.
We are witnessing a paradigm shift in drug development and clinical practice to fight the novel coronavirus disease (COVID-19), and a number of clinical trials have been or are being testing various pharmacological approaches to counteract viral load and its complications such as cytokine storm. However, data on the effectiveness of antiviral and immune therapies are still inconclusive and inconsistent. As compared to other candidate drugs to treat COVID-19, Janus Kinase (JAK) inhibitors, including baricitinib and ruxolitinib, possess key pharmacological features for a potentially successful repurposing: convenient oral administration, favorable pharmacokinetic profile, multifunctional pharmacodynamics by exerting dual anti-inflammatory and anti-viral effects. Baricitinib, originally approved for rheumatoid arthritis, received Emergency Use Authorization in November 2020 by the Food and Drug Administration in combination with remdesivir for the treatment of COVID-19 in hospitalized patients >= 2 years old who require supplemental oxygen, invasive mechanical ventilation, or extracorporeal membrane oxygenation. By July 2021, the European Medicines Agency is also expected to issue the opinion on whether or not to extend its use in hospitalised patients from 10 years of age who require supplemental oxygen. Ruxolitinib, approved for myelofibrosis, was prescribed in patients with COVID-19 within an open-label Emergency Expanded Access Plan. This review will address key milestones in the discovery and use of JAK inhibitors in COVID-19, from artificial intelligence to current clinical evidence, including real world experience, and critically appraise emerging safety issues, namely infections, thrombosis, and liver injury. An outlook to ongoing studies (ClinicalTrials.gov) and unpublished pharmacovigilance data is also offered.

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