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. 2022 Jul 18;16:e187430642205230. doi: 10.2174/18743064-v16-e2205230

Table 3.

Biologics for the treatment of Th2-high asthma.

- 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