Abstract

BackgroundPatients with severe, uncontrolled asthma have a significant unmet need for new treatments that have broader effects on airway inflammation, and that provide greater improvements in asthma outcomes than currently approved biologics and standard-of-care therapies. Tezepelumab is a human monoclonal antibody that blocks the activity of the epithelial cytokine thymic stromal lymphopoietin. In the PATHWAY phase 2b study (NCT02054130), tezepelumab significantly reduced exacerbations by up to 71% in adults with severe, uncontrolled asthma, irrespective of baseline disease phenotype. This article reports the design and objectives of the pivotal phase 3 NAVIGATOR study.MethodsNAVIGATOR (NCT03347279) is an ongoing randomized, double-blind, placebo-controlled trial in adults (18–80 years old) and adolescents (12–17 years old) with severe, uncontrolled asthma, who are receiving treatment with medium- or high-dose inhaled corticosteroids plus at least one additional controller medication with or without oral corticosteroids (N = 1061). The study population includes approximately equal proportions of patients with high (≥ 300 cells/μL) and low (< 300 cells/μL) blood eosinophil counts. The study comprises a 5–6-week screening period, a 52-week treatment period and a 12-week post-treatment follow-up period. All patients will receive their prescribed controller medications without change throughout the study. The primary efficacy endpoint is the annualized asthma exacerbation rate during the 52-week treatment period. Key secondary endpoints include the effect of tezepelumab on lung function, asthma control and health-related quality of life.DiscussionNAVIGATOR is evaluating the effect of tezepelumab in patients with a broad range of severe asthma phenotypes at baseline, including those with low blood eosinophil counts. The target sample size for NAVIGATOR (N = 1060) was achieved, and it is the largest clinical study of tezepelumab in severe, uncontrolled asthma to date. NAVIGATOR aims to further investigate the effect of tezepelumab on exacerbations and build on observations from the phase 2b PATHWAY study, and to demonstrate further the potential of tezepelumab to provide patients with severe, uncontrolled asthma with improvements in lung function, asthma control and health-related quality of life.Trial registrationNCT03347279 (ClinicalTrials.gov). Registered 20 November 2017.

Highlights

  • Patients with severe, uncontrolled asthma have a significant unmet need for new treatments that have broader effects on airway inflammation, and that provide greater improvements in asthma outcomes than currently approved biologics and standard-of-care therapies

  • Available biologic therapies for severe asthma target immunoglobulin (Ig) E, interleukin (IL) -4 receptor α/IL-13, IL-5 and IL-5 receptor α [8]. These treatments have an indication limited to patients with: an eosinophilic phenotype; an allergic phenotype; or severe asthma with type 2 inflammation characterized by raised blood eosinophil counts and/or raised fractional exhaled nitric oxide (FeNO) levels [9,10,11,12,13,14]

  • The need for such a treatment is pertinent for patients with low blood eosinophil counts, including those with type 2-low inflammation, for patients whose asthma is driven by multiple inflammatory pathways, and for patients who do not respond well to treatment with existing biologic therapies

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Summary

Introduction

Patients with severe, uncontrolled asthma have a significant unmet need for new treatments that have broader effects on airway inflammation, and that provide greater improvements in asthma outcomes than currently approved biologics and standard-of-care therapies. Clinical studies have demonstrated that these treatments decrease exacerbation rates by approximately 50%, and that they provide variable improvements in lung function and symptom scores in some patients [15,16,17,18] An explanation for this lack of complete efficacy may be that currently available biologics target individual cytokines or cell types, leaving other components of the asthma inflammatory response untreated. Targeting an upstream mediator of inflammation that is triggered early in the inflammatory response, and that activates a higher number of different inflammatory pathways, cytokines and cells than downstream inflammatory mediators, may have a broader effect on airway inflammation and may provide more effective asthma control The need for such a treatment is pertinent for patients with low blood eosinophil counts, including those with type 2-low inflammation, for patients whose asthma is driven by multiple inflammatory pathways, and for patients who do not respond well to treatment with existing biologic therapies

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