Table 1.
Drug treatment | Mode of action | Patient category | Primary endpoint | Estimated | Trial/phase (as | Testing status |
---|---|---|---|---|---|---|
enrollment | of 07/18/2021) | |||||
XPro1595 | Soluble TNF inhibitor | COVID-19 with pulmonary complications | The proportion of participants who die or require mechanical ventilation. | 366 | NCT04370236, phase 2/3 | Recruiting |
CERC-002 | LIGHT(TNFSF14) inhibitor | COVID-19 with mild to moderate ARDS | The proportion of patient alive and free of respiratory failure | 82 | NCT04412057, phase 2 | Completed |
Infliximab | Chimeric monoclonal anti-TNF antibody | COVID-19 | Time to improvement in oxygenation | 17 | NCT04425538, phase 2 | Completed |
Chimeric monoclonal anti-TNF antibody | COVID-19 | 28-day mortality | 88 | NCT04922827, phase 2 | Recruiting | |
Tocilizumab /Infliximab | TNFα inhibitor (Infliximab) | COVID-19-associated Cytokine Storm Syndrome | Time to improvement in oxygenation | 84 | NCT04734678 | Recruiting |
Adamumab (Qletli) | TNFα inhibitor | Severe and critical COVID-19 | Time to clinical improvement | 30 | ChiCTR2000030089 | Not yet recruiting |
Infliximab/vedolizumab | TNFα inhibitor (infliximab) | IBD and COVID-19 | IgG and IgM anti SARS-CoV-2 | 850 | NCT04344249 | Recruiting |