
Masitinib Shows Promise in Reducing Severe Asthma Exacerbations
The first-in-class drug in severe asthma significantly reduced the exacerbation rate by 35% compared with placebo.
According to a new phase 3 study, masitinib significantly decreased the rate of
These findings will be presented this week at an American Thoracic Society (ATS 2020) symposium as a late breaking clinical trial.
The AB07015 study, led by Pascal Chanez, MD, PhD, Professor of Respiratory Diseases, Aix-Marseille University, France, was a randomized, double-blinded, placebo-controlled trial that evaluated the efficacy of 6 mg/kg/day of masitinib treatment for severe persistent asthma.
Masitinib is a first-in-class drug in severe asthma that selectively targets mast cells through inhibition of tyrosine kinases c-Kit, LYN, and FYN. Previous research has demonstrated the therapeutic potential of and rationale for targeting mast cells in asthma.
However, the AB07015 trial was the first positive large-scale study in severe asthma utilizing a drug of this kind.
In the study, they enrolled a total of 355 patients in their primary analysis population. They especially noted patients with an initial eosinophil count of ≥150 cells/μL, which the investigators considered a key subgroup for their analysis.
Following enrollment, patients were randomized 2:1 to receive either masitinib or placebo for 36 weeks, with a possible extension period until at least week 96.
Baseline characteristics and average exposure times (60 weeks) were well-balanced across treatment arms, the investigators noted.
Thus, the primary endpoint for the study was a reduction of annualized severe asthma exacerbation rate for overall exposure. They defined a severe asthma exacerbation event as worsening asthma leading to an increase from stable maintenance dose of corticosteroids for ≥3 days or hospitalization.
Following the treatment period, Chanez and team reported that masitinib significantly reduced the severe asthma exacerbation rate by 35% compared with placebo (rate ratio, 0.64 [95% CI, 0.48-0.84; P = .0014]).
Additionally, the eosinophil ≥150 cells/μL subpopulation demonstrated a significant reduction in severe exacerbations by 38% (rate ratio, 0.69 [95% CI, 0.49-0.95; P = .0249]).
The investigators also assessed a safety population — which included 404 patients, all of whom received at least 1 dose of the investigative drug, which included low-dosage (≤5mg/day).
In this population, 83.4% of masitinib users experienced ≥1 adverse events—compared with 82.0% in placebo users.
The rates for serious and severe adverse events for masitinib were 17.7% and 16.5%, respectively. For placebo, these rates were 48.0% and 45.9%, respectively.
“Masitinib, a first-in- class tyrosine kinase inhibitor targeting mast cell activity in severe asthma patients, demonstrated a positive benefit/risk ratio over a sustained period and may provide a new treatment option in severe asthma, irrespective of baseline eosinophil level,” the investigators concluded.
The study, “











































































