Table 3.
- | Omalizumab (XOLAIR) | Mepolizumab (NUCALA) | Reslizumab (CINQAIR) | Benralizumab (FASENRA) | Dupilumab (DUPIXENT) |
---|---|---|---|---|---|
FDA approval | Moderate-to-severe persistent asthma in ≥6 years, with a positive skin test or in vitro reactivity to a perennial aeroallergen and symptoms that are inadequately controlled with inhaled corticosteroids | Add-on maintenance treatment for ≥6 years with severe asthma and eosinophilic phenotype | Add-on maintenance treatment for ≥18 years with severe asthma and eosinophilic phenotype | Add-on maintenance treatment for ≥12 years with severe asthma and eosinophilic phenotype | Add-on maintenance treatment for moderate-to-severe asthma ≥12 years with an eosinophilic phenotype or with oral-corticosteroid-dependent asthma |
Target | IgE | IL5 | IL5 | IL5 receptor | IL4 receptor |
Route of administration | Subcutaneous | Subcutaneous | Intravenous infusion over 20–50 minutes | Subcutaneous | Subcutaneous |
Frequency of administration | Every 2–4 weeks | Every 4 weeks | Every 4 weeks | Every 4 weeks for three doses, then every 8 weeks | Every 2 weeks |
Dose | Based on body weight and pretreatment serum IgE | 40 mg for 6–11 years; 100 mg for ≥12 years | 3 mg/kg body weight | 30 mg | Initial dose 400 mg followed by doses of 200 mg Or initial dose 600 mg followed by doses of 300 mg |
Benefits | Fewer exacerbations and decreased need for ICS and rescue treatment [77] Improvement in asthma-related quality of life [78] compared with placebo |
Reduced rate of exacerbations and reduced hospitalization or ER visits associated with exacerbations [79] Reduction in dose of OCS [80] compared with placebo |
Reduced rate of asthma exacerbations [81] Enhanced asthma-related quality of life, lung function, and asthma control [82] versus placebo |
Reduced frequency of exacerbations. Improved lung function and symptoms [83] Reduced OCS use [84] compared with placebo |
Reduced number of exacerbations, improved lung function and asthma control [85] Reduction in OCS dose [86] compared with placebo |
Adverse events as per label | Injection site reactions, viral infections, upper respiratory tract infection, sinusitis, headache, and pharyngitis | Headache, injection site reaction, back pain, and fatigue | Oropharyngeal pain | Headache and pharyngitis | Injection site reactions, conjunctivitis, blepharitis, oral herpes, keratitis, eye pruritus, other herpes simplex virus infection, and dry eye |
Availability in the Gulf | Yes | Yes | No | Yes | Yes |