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Active NON-SBIR/STTR RPGS NIH (US)

Clinical trial of omalizumab for allergen sensitized and exposed individuals with COPD

$25.21M USD

Funder NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES
Recipient Organization Johns Hopkins University
Country United States
Start Date Aug 15, 2024
End Date May 31, 2031
Duration 2,480 days
Number of Grantees 2
Roles Co-Investigator; Principal Investigator
Data Source NIH (US)
Grant ID 10927604
Grant Description

Project Summary Chronic Obstructive Pulmonary Disease (COPD) is a heterogeneous disease with significant variation in disease manifestation, progression, and outcomes. There is increasing interest in precision medicine strategies in COPD to identify disease traits that, when targeted for treatment, result in improved outcomes. There has

been increasing recognition of the prevalence of allergic disease and allergic sensitization in COPD, but the clinical significance of this overlapping trait has been unclear. Blood eosinophils have been recognized as a trait to help target treatment with inhaled corticosteroids among individuals with COPD but are imprecise as a

biomarker of type 2 inflammation. We recently published compelling results showing that individuals with COPD having both allergic sensitization as well as concomitant exposure to common indoor aeroallergens, also having elevated total IgE, have a substantially higher risk of adverse outcomes. It is also well established

that individuals with allergic asthma having sensitization with exposure to common indoor aeroallergens have significant benefit from treatment with omalizumab. Accordingly, we propose the Clinical trial of omalizumab for allergen sensitized and exposed individuals with COPD (COPD OMA) a masked, randomized, placebo-

controlled multi-center phase 2 clinical trial of omalizumab versus placebo among individuals with COPD having sensitization with concomitant exposure to common indoor allergens. The trial will enroll 330 individuals with moderate to severe COPD in partnership with the American Lung Association-Airways Clinical Research

Centers (ALA-ACRC) and will test whether omalizumab leads to treatment response, including improvement in exacerbation risk (primary outcome), disease status (measured by St. George's Respiratory Questionnaire and COPD Assessment Test Score), and lung function (secondary outcomes) over the course of 12 months. The

study will be conducted at twenty centers throughout the US. In a mechanistic aim, we also propose to explore molecular signatures of IL-4 and IL-13 cytokines to understand drivers of disease morbidity as well as treatment response in this population. Accordingly, this is an ideal phase II clinical trial with the goals of

detecting a signal for efficacy of omalizumab in improving relevant clinical outcomes among a high-risk subgroup of individuals; and understanding relevant biologic endotypes with increased responsiveness to treatment.

All Grantees

Johns Hopkins University

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