We remind investors, that last November, tezepelumab met the primary endpoint in the phase III NAVIGATOR study which evaluated the candidate for treating patients with severe, uncontrolled asthma.
The FDA granted Breakthrough Therapy designation to tezepelumab for the treatment of patients with severe, uncontrolled asthma without an eosinophilic phenotype in September 2018.
Competitive pressure in the overall asthma market has intensified over the years. Upon potential approval, tezepelumab is likely to face stiff competition from GlaxoSmithKline’s GSK Nucala and Regeneron REGN/Sanofi’s blockbuster medicine Dupixent, which are approved for treating patients with severe asthma and some other indications as well.