Efficacy, safety and tolerability of GSK2190915, a 5-lipoxygenase activating protein inhibitor, in adults and adolescents with persistent asthma: a randomised dose-ranging study.

Abstract

BACKGROUND:

GSK2190915 is a high affinity 5-lipoxygenase-activating protein inhibitor being developed for the treatment of asthma. The objective of this study was to evaluate GSK2190915 efficacy, dose-response and safety in subjects with persistent asthma treated with short-acting beta2-agonists (SABAs) only.

METHODS:

Eight-week multicentre, randomised, double-blind, double-dummy, stratified (by age and smoking status), parallel-group, placebo-controlled study in subjects aged ≥12 years with a forced expiratory volume in 1 second (FEV1) of 50-85% predicted. Subjects (n = 700) were randomised to receive once-daily (QD) oral GSK2190915 (10-300 mg), twice-daily inhaled fluticasone propionate 100 μg, oral montelukast 10 mg QD or placebo. The primary endpoint was mean change from baseline (randomisation) in trough (morning pre-dose and pre-rescue bronchodilator) FEV1 at the end of the 8-week treatment period. Secondary endpoints included morning and evening peak expiratory flow, symptom-free days and nights, rescue-free days and nights, day and night-time symptom scores, day and night-time rescue medication use, withdrawals due to lack of efficacy, Asthma Control Questionnaire and Asthma Quality of Life Questionnaire scores.

RESULTS:

For the primary endpoint, there was no statistically significant difference between any dose of GSK2190915 QD and placebo. However, repeated measures sensitivity analysis demonstrated nominal statistical significance for GSK2190915 30 mg QD compared with placebo (mean difference: 0.115 L [95% confidence interval: 0.00, 0.23], p = 0.044); no nominally statistically significant differences were observed with any of the other doses. For the secondary endpoints, decreases were observed in day-time symptom scores and day-time SABA use for GSK2190915 30 mg QD versus placebo (p ≤ 0.05). No dose-response relationship was observed for the primary and secondary endpoints across the GSK2190915 dose range studied; the 10 mg dose appeared to be sub-optimal. GSK2190915 was associated with a dose-dependent reduction in urinary leukotriene E4. The profile and incidence of adverse events were similar between treatment groups.

CONCLUSION:

Efficacy was demonstrated for GSK2190915 30 mg compared with placebo in day-time symptom scores and day-time SABA use. No additional improvement on efficacy endpoints was gained by administration of GSK2190915 doses greater than 30 mg. GSK2190915 was well-tolerated. These results may support further studies with GSK2190915 30 mg.

TRIAL REGISTRATION:

Clinicaltrials.gov: NCT01147744.

• Authors: Richard M A Follows, Neil G Snowise, Shu-Yen Ho, Claire L Ambery, Kevin Smart, Barbara A McQuade
• Journal: Respiratory research (Respir Res) Vol. 14 Pg. 54 (May 17 2013) ISSN: 1465-993X [Electronic] England
• PMID: 23682661 (Publication Type: Clinical Trial, Phase II, Journal Article, Multicenter Study, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)

Chemical References

• 3-(3-tert-butylsulfanyl-1-(4-(6-ethoxypyridin-3-yl)benzyl)-5-(5-methylpyridin-2-ylmethoxy)-1H-indol-2-yl)-2,2-dimethylpropionic acid
• 5-Lipoxygenase-Activating Protein Inhibitors
• Adrenergic beta-2 Receptor Agonists
• Anti-Asthmatic Agents
• Indoles
• Pentanoic Acids

Topics

• 5-Lipoxygenase-Activating Protein Inhibitors (administration & dosage, adverse effects, therapeutic use)
• Adolescent
• Adrenergic beta-2 Receptor Agonists (therapeutic use)
• Adult
• Aged
• Anti-Asthmatic Agents (administration & dosage, adverse effects, therapeutic use)
• Asthma (drug therapy)
• Child
• Dose-Response Relationship, Drug
• Double-Blind Method
• Female
• Forced Expiratory Volume
• Humans
• Indoles (administration & dosage, adverse effects, therapeutic use)
• Male
• Middle Aged
• Pentanoic Acids (administration & dosage, adverse effects, therapeutic use)
• Smoking (adverse effects)
• Treatment Outcome
• Young Adult