Table 1.
Conventional and biologic DMARDs involved in therapeutic research for COVID19 (updated at June 18,2020).
Drugs | Rational | Population/Condition | Trials Status/RCTs with results (number) |
---|---|---|---|
Chloroquine/Hydroxycloroquine | Anti-inflammatory and immunomodulatory effects, both on adaptive and innate immunity, with inhibition of cytokine, leukotrienes, prostaglandins, proteases and oxyradicals production. It also interfers with lysosomal activity and autophagy, membrane stability and signaling pathways and transcriptional activity, which can result in modulation of certain costimulatory molecules and may interfere with viral infection and replication. Inhibition pH-dependent steps of the replication of several viruses, including SARS-CoV infection. Modulation of glycosylation of cellular receptors of SARS-CoV | From preventative treatment to severe forms of COVID-19, including COVID19-pneumonia | Recruiting or Authorized/0 |
Leflunomide | Tyrosine kinase inhibition, Inhibition of pyrimidine de novo synthesis | COVID19-pneumonia | Recruiting or Authorized/0 |
Cyclosporin a | Calcineurin inhibitor. It can inhibit the replication of several coronaviruses, including SARS-COV | Hospitalized COVID19 patients, COVID19-pneumonia | Authorized/0 |
Tocilizumab | Immunosuppressive effect with IL6-inhibition, efficacy in cytokine release syndrome | COVID19, severe COVID19, COVID19-pneumonia | Recruiting or Authorized/0 |
Sarilumab | Immunosuppressive effect with IL6-inhibition | Moderate-severe COVID19, Hospitalized COVID19 patients, COVID19-pneumonia | Authorized/0 |
Anakinra | Immunosuppressive effect with IL1-inhibition, inhibition of the inlammasome | COVID19, COVID19-pneumonia, Cytokine storm syndrome in COVID19 | Authorized/0 |
Canakinumab | Immunosuppressive effect with IL1-inhibition, inhibition of the inlammasome | COVID19-pneumonia | Authorized/0 |
Adalimumab | Immunosuppressive effect with TNFalpha-inhibition | Severe COVID19-pneumonia | Not Recruiting/0 |
Ixekizumab | Immunosuppressive effect with IL17-inhibition. IL17 functions are crucial in different settings of viral infections. For MERS-CoV, SARS-CoV and SARS-CoV-2, the severity of disease was shown to positively correlate with levels of IL-17. The excessive production of IL-17 has been observed in patients with ARDS | COVID19-pneumonia | Recruiting/0 |
Baricitinib | Inhibition of JAK/STAT pathway, reduction of proinflammatory cytokines, potential inhibition of AP2 associated proteinkinase1 (AAK1) that SARS-CoV-2 uses to infect lung cells through binding with ACE2 | COVID19-pneumonia | Authorized/0 |
Ruxolitinib | Inhibition of JAK/STAT pathway, reduction of proinflammatory cytokines | COVID19, severe COVID19, severe COVID19-pneumonia, COVID19-ARDS, Cytokine storm syndrome in COVID19 | Recruiting or Authorized/0 |
Jakotinib | Inhibition of JAK/STAT pathway, reduction of proinflammatory cytokines | Severe and acute exacerbation COVID19-pneumonia | Recruiting/0 |