Table 1 Selected current treatments for non-pregnant adult patients hospitalized for COVID-19 (adapted from ref.153, Springer Nature Limited)
Immunothrombosis therapy | Drug/target | Treatments and responses | Limits/recommendations | Refs. |
|---|---|---|---|---|
Corticosteroids | Dexamethasone | Hospitalized patients; increases organ support-free days and reduces 28-day mortality | Recommended | |
Janus kinase (JAK) inhibitors | Baricitinib (with IL-6 inhibitor and dexamethasone) | Patients with moderate–severe illness; rapid declines of C-reactive protein, ferritin and D-dimer with gradual improvement in haemoglobin, platelet counts and clinical status | At least 2 large RCTs; high likelihood of benefit | |
IL-6 inhibitors | Toclizumab | Hospitalized patients; reduces inflammatory markers, D-dimer and fibrinogen; reduced 21 or 28-day mortality and organ support-free days | For critically and severely ill patients; widely used | |
Anticoagulants | Low molecular weight heparin (LMWH) — prophylactic intensity | Critically ill patients (hospitalized, intensive care unit) for venous thromboemboli prophylaxis and to increase the number of organ support-free days; no effect on survival to hospital discharge | Certainty of evidence from multiple trials is low; but widely used | |
LMWH — therapeutic dose | Patients with moderate-severity illness (hospitalized, low-flow oxygen use, elevated D-dimer) for venous/arterial thromboemboli prophylaxis and to reduce organ support-free survival; uncertain if an effect on survival; consider bleeding risk | Certainty of evidence from multiple trials is low; but widely used | ||
Rivaroxaban (or other direct oral anticoagulants) | Patients with moderate-severity illness; no effect on survival or need for supplemental oxygen | Not recommended | ||
Anti-platelets | Aspirin, P2Y12 inhibitors | Early use of ASA may lower odds of 28-day in-hospital mortality; no benefit from P2Y12 inhibitors | Not recommended | |
Thrombolytics | Alteplase (tPA) | For respiratory failure with heparin; evidence of moderate improved oxygenation | Early phase | |
Anti-spike protein monoclonal antibodies | Casirivumab and imdevimab | Hospitalized patients; may reduce 28-day mortality | Uncertain which patient groups will benefit most | |
Anti-complement | Inhibitor of C5 activation: ravulizumab | Critically ill patients, phase III study; stopped due to lack of clinical benefit | No clinical benefit | |
Inhibitor of C5 activation: zilucoplan | Patients with moderate-severity illness; improved oxygenation at day 15, reduced cytokine levels and reduced 28-day mortality | Underpowered | ||
C5a blockade: (e.g., violbelimab, BDB-001); C5a-receptor blockage (avdoralimab) | Hospitalized patients; evidence of improvements in oxygenation | Early phase or underpowered studies | ||
C3 inhibitors (e.g., AMY-101, APL9), C1-esterase inhibitor, MASP2 antibody (narsoplimab) | Hospitalized patients; evidence of improvements in oxygenation | Early phase or underpowered studies | ||
Bradykinin-targeted | Icatibant (bradykinin 2 receptor antagonist), ecallantide (kallikrein inhibitor) | Icatibant ± C1-esterase inhibitor; evidence of improvements in oxygenation | Underpowered |