Table I.
Agent | Clinical trial status | Efficacy | References |
---|---|---|---|
Anti-cytokine therapies | |||
IL-4R-α antagonist | Phase 2 | Despite initial benefits in severe asthmatics, these compounds have been discontinued | 27 |
Anti-IL-5 | Phase 2 | Shown to reduce the number of severe asthma exacerbations | 24, 25 |
Anti-IL-5R-α | Phase 2 | Reduces circulating eosinophils. Favourable safety, pharmacokinetic and pharmacodynamic profile. Efficacy studies using IV and SC routes of administration still ongoing | 13 |
Anti-IL-9 | Phase 2b | Modest improvements reported in patients with mild asthma undergoing allergen challenge. Larger clinical studies underway in severe asthmatics | 14 |
Anti-IL-13 | Phase 2 | Five anti-IL-13 compounds investigated. Early compounds reduced both early asthmatic response (EAR) and late asthmatic response (LAR) Majority of Phase 2 results yet to be released |
15, 16 |
Chemokine ihibitors | |||
CCR3 antagonist | Phase 2 | Orally active competitive antagonist, currently on trial for mild to moderate asthma | 17 |
Toll-like receptor targets | |||
TLR7, TLR9 synthetic agonists | Phase 1 and 2 | Effective in animal models of asthma, efficacy in human studies yet to be determined | 18 |
Kinase inhibitors | |||
Syk kinase inhibitor | Phase 2 planned | In Phase 1, reported that the inhaled inhibitor is well tolerated, with an improvement in both the EAR and LAR | 19 |
c-kit/PDGF receptor tyrosine kinase inhibitor | Phase 3 | In Phase 2, generated promising efficacy data and good safety profile | 20 |
Phosphodiesterase inhibitors | |||
PDE 3/4 inhibitors | Phase 2 | Reduced EAR and LAR in naive atopic asthmatics in response to inhaled allergen. However, orally administered drugs result in side effects such as gastro-intestinal symptoms | 21 |