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Written and prepared by:
Eleni Karakike, George N. Dalekos, Ioannis Koutsodimitropoulos, Maria Saridaki, Chryssa Pourzitaki, Georgios Papathanakos, Antigone Kotsaki, Stamatios Chalvatzis, Vasiliki Dimakopoulou, Nikolaos Vechlidis, Elisabeth Paramythiotou, Christina Avgoustou, Aikaterini Ioakeimidou, Elli Kouriannidi, Apostolos Komnos, Evangelia Neou, Nikoletta Rovina, Eleni Stefanatou, Haralampos Milionis, George Nikolaidis, Antonia Koutsoukou, Georgia Damoraki, George Dimopoulos, Vassileios Zoumpos, Jesper Eugen-Olsen, Karolina Akinosoglou, Nikolaos K. Gatselis, Vasilios Koulouras, Eleni Gkeka, Nikolaos Markou, Mihai G. Netea, Evangelos J. Giamarellos-Bourboulis
Delve into the ESCAPE trial, an open-label phase II study investigating personalized immunotherapy for critically ill COVID-19 patients. Patients were treated with anakinra or tocilizumab based on immune function tests. Findings suggest anakinra provided more clinical benefit in reducing organ dysfunction, particularly for patients with macrophage activation syndrome (MAS) or complex immune dysregulation (CID) with increased aminotransferases.
Open-label trial shows personalized immunotherapy using anakinra and tocilizumab improves outcomes in critically ill COVID-19 patients.
Study compares the effectiveness of anakinra and tocilizumab in treating severe COVID-19 cases, showing better outcomes with anakinra.
Utilizing immune function tests to guide personalized immunotherapy for critically ill COVID-19 patients.
Ferritin and HLA-DR levels used to determine the appropriate immunotherapy for severe COVID-19 patients.
Anakinra treatment linked to improved clinical outcomes and reduced severity in critically ill COVID-19 patients.
Study finds anakinra more effective than tocilizumab in reducing SOFA scores and improving respiratory function in severe COVID-19 cases.
Insurance covers clinical consultations.
Subscription fee (from $59/month not billed to insurance) covers immunotherapy, shipping & related costs.