Table 1.
Compound | Target Molecule | FDA Approval Date | Administration Route | Dosage | Ideal Patients | Principal Outcomes |
---|---|---|---|---|---|---|
Mepolizumab | Inhibit IL-5, preventing its binding with the α chain of the receptor present on the surface of the eosinophils | 4-Nov-15 | Subcutaneous | 100 mg every 4 weeks | Eosinophilic asthma ≥ 300 cells/µL, CRSwNP, late onset asthma | Excellent safety profile, clinical efficacy and steroid sparing effect |
Benralizumab | Bind to the α-chain of the IL-5R with inhibition of receptor activation mediated by IL-5 | 14-Nov-17 | Subcutaneous | Every 4 weeks for the first 3 doses, then every 8 weeks | Eosinophilic asthma ≥ 300 cells/µL, CRSwNP, late onset asthma | High affinity for IL-5 receptor and ADCC activity, eosinophils sustained tissue depletion, improvement of pulmonary function even in patients with FAO |
Reslizumab | Block IL - 5, inhibiting the binding and interaction with its receptors | 23-Mar-16 | Intravenous | 3 mg · kg -1 | Eosinophilic asthma ≥ 400 cells/µL, CRSwNP | Personalized dosage, improvement of pulmonary function |
Dupilumab | Direct against α subunit of the IL-4R, capable of blocking the signaling of IL-4 and IL-13 | 28-Mar-18 | Subcutaneous | 200/300 mg every two weeks | FeNO ≥ 25 ppb and eosinophilic asthma ≥ 150 cells/µL | Reduction in severe exacerbations and in average dose of OCS, improvement in lung function (FEV1 l) |
Omalizumab | Bind free IgE, blocking its interaction with FcεRI on basophils, mast cells and dendritic cells | 20-Jun-2003 | Subcutaneous | Doses up 600 mg every two weeks | Allergic, patients with total serum IgE levels ≥ 30 and ≤ 1500 kU/l | Reduction in frequency of asthma exacerbation, improvement QoL and reduction use of OCS |
Abbreviations: ADCC, antibody-dependent cell cytotoxicity; FAO, fixed airway obstruction; CRSwNP, chronic sinusitis with nasal polyps; FeNO, fractional exhaled nitric oxide.