Title
Effects of Anti-TSLP in Patients With Asthma
Effects of Anti-TSLP on Airway Hyperresponsiveness and Mast Cell Phenotype in Asthma - A Randomized Double-blind, Placebo-controlled Trial of MEDI9929
Phase
Phase 2Lead Sponsor
University Hospital Bispebjerg and FrederiksbergStudy Type
InterventionalStatus
Completed No Results PostedIndication/Condition
AsthmaIntervention/Treatment
tezepelumab ...Study Participants
40The purpose of this study is to determine whether anti-TSLP will decrease airway hyperresponsiveness in patients with asthma already on daily treatment with inhaled corticosteroids.
The investigators expect that airway hyperresponsiveness will decrease after treatment with anti-TSLP, and that this happens due to a change in the type of mast cells with in the lungs. Also, the investigators expect a decrease in inflammatory cells and mediators measured in material from the lungs.
Half of the participants will receive anti-TSLP (MEDI9929) on top of their regular asthma treatment, while the other half will receive placebo on top of their regular asthma treatment.
The mannitol test is increasingly used by clinicians to diagnose asthma. It has clinical advantages in terms of being feasible in a wide range of settings with the need of a minimum of equipment. Airway hyper responsiveness (AHR) to mannitol correlates with eosinophilic airway inflammation and the degree of asthma control, predicts the risk of exacerbation and response to inhaled steroids.
Subjects with asthma and indirect AHR have increased levels of intraepithelial carboxypeptidase A3 (CPA3), a metalloexopeptidase specifically expressed by mast cells, compared to asthmatics without AHR. CPA3 is known to be selectively present in the MCTC phenotype (mast cells containing both tryptase and chymase), and recent studies suggest that increased CPA3 levels also constitutes a marker of a Th2-high/eosinophilic and steroid-responsive asthma. Interestingly, treating mast cell precursors with TSLP increases CPA3 immunostaining, suggesting that TSLP released by e.g. airway epithelium up-regulate a mast cell phenotype that is potentially important in AHR and also promotes eosinophilic airway inflammation. Previous published data by the investigators confirm that increased MCTC in submucosa of subjects with asthma is associated with an increased CPA3 and TSLP expression.
The investigators speculate that the effect of MEDI9929 on AHR to mannitol is likely to be primarily a consequence of functional differences in mast cells. Treating subjects with asthma with MEDI9929 will potentially block downstream effects on mast cell activation as well as eosinophilic inflammation, which may reduce AHR to inhaled mannitol.
The purpose of this study is to investigate whether AHR to mannitol is a suitable marker of response to MEDI9929, but also to better understand the anti-inflammatory effects of MEDI9929 in the lungs, including whether a reduced AHR to mannitol following treatment with MEDI9929 is related to a reduction in chymase/CPA-3 positive mast cells. The investigators hypothesize that MEDI9929 will decrease the response to mannitol (measured as an increase in PD15) after 12 weeks of treatment as compared to placebo. It is further hypothesized that the number of chymase/CPA-3 positive mast cells in airway epithelium and submucosa will be reduced after 12 weeks of treatment with MEDI9929 in subjects with AHR to mannitol.
This trial offers the opportunity to study potential biomarkers and surrogate endpoints, but also to identify the anti-inflammatory effects of MEDI9929 on a mechanistic level.
This study is a randomized, double-blind, placebo-controlled trial. It includes a enrolment period of maximum 2 weeks, 12 weeks of treatment (three IV doses of either 700mg MEDI9929 or placebo) and 8 weeks follow-up after the second bronchoscopy.
MEDI9929 700mg (3 doses in total, 4-week intervals), administered intravenously
Placebo (3 doses in total, 4-week intervals), administered intravenously
MEDI9929 is a human monoclonal antibody immunoglobulin IgG2λ directed against TSLP. MEDI9929 binds with human TSLP and prevents its interaction with thymic stromal lymphopoietin receptor (TSLPR).
Apart from the active substance, the placebo is otherwise identical to IMP.
Inclusion Criteria: Written informed consent Age 18 through 75, inclusive at the time of Visit 1 Body mass index between 18-40 kg/m2 (both inclusive) and weight ≥ 40 kg at Visit 1. A diagnosis of asthma as defined by GINA (ginasthma.org). ICS (in any dose) on a daily basis for at least three months prior to Visit 1 A stable asthma controller regimen with ICS (±LABA) for at least 4 weeks prior to Visit 1 A FEV1 value of ≥ 70% at Visit 1 ACQ-6 > 1 (partly controlled) at Visit 1 PD15 to mannitol <= 315 mg at visit 1 Subjects must demonstrate acceptable inhaler and spirometry techniques during screening (as evaluated and in the opinion of study site staff) Subjects must demonstrate ≥ 70% compliance with usual asthma controller ICS±LABA during the screening (V1 to V3). Exclusion Criteria: Current smokers or subjects with a smoking history of ≥ 10 pack years. Former smokers with < 10 pack years must have stopped for at least 6 months to be eligible. Previous medical history or evidence of an uncontrolled intercurrent illness. Any concomitant respiratory disease that in the opinion of the investigator and/or medical monitor will interfere with the evaluation of the investigational product or interpretation of subject safety or study results. Clinically relevant abnormal findings in hematology or clinical chemistry. Evidence of active liver disease. History of cancer. Acute upper or lower respiratory infections. Helminth parasitic infection. Known history of active tuberculosis (TB). Positive hepatitis B surface antigen, or hepatitis C virus antibody serology. A positive human immunodeficiency virus (HIV) test. History of sensitivity to any component of the investigational product. History of anaphylaxis to any biologic therapy. History of documented immune complex disease (Type III hypersensitivity reactions) to mAb administration. History of any known primary immunodeficiency disorder. Oral corticosteroids. Use of 5-lipoxygenase inhibitors. Use of immunosuppressive medication. Pregnant, breastfeeding or lactating females. History of chronic alcohol or drug abuse. Receipt of the Th2 cytokine inhibitor suplatast Receipt of any live or attenuated vaccines.
