First author [ref.] | Drug | Subjects n | Primary end-point | Duration | Main findings |
Leckie [13] | Mepolizumab | 24 | Histamine AHR | Single dose | Decreased blood eosinophils up to 16 weeks, no significant effect on AHR |
Büttner [4] | Mepolizumab | 19 | Eosinophil population and ECP levels | 12 weeks | Decreased eosinophils and serum ECP |
Flood-Page [35] | Mepoliumab | 24 | Airway eosinophils and clinical parameters of disease activity | 8 weeks | Decreased airway eosinophils, no change in clinical parameter |
Flood-Page [36] | Mepolizumab | 362 | Clinical parameters | 12 weeks | No change in clinical end-points Trend for a reduction in exacerbation rate |
Haldar [37] | Mepolizumab | 61 | Exacerbations | 12 months | Significant reduction in severe exacerbations and improvement of the AQLQ score |
Nair [38] | Mepolizumab | 20 | Exacerbations and prednisone sparing effect | 5 months | Reduction of oral steroid daily dose without exacerbations |
Pavord [39] | Mepolizumab | 621 | Exacerbations | 12 months | Significant decrease of the exacerbation rates |
Kips [40] | Reslizumab | 26 | Symptoms | Single dose | No modification of symptoms |
Castro [41] | Reslizumab | 106 | ACQ score | 12 weeks | No change in ACQ score, pulmonary function tests or clinical parameters Significant decrease of sputum eosinophilia |
Busse [42] | Benralizumab | 44 | Safety in an open-labelled study | Single dose | No serious adverse events |
AHR: airway hyperresponsiveness; ECP: eosinophil cationic protein; ACQ: asthma control questionnaire; AQLQ: Asthma Quality of Life Questionnaire.