Clinical trial

Effects of IL-4R-alpha Inhibition (Dupixent) Inhibition On The Respiratory Microbiome And Immunologic Correlates In Patients With Severe Asthma

Name
HUM00196809
Description
The overall goal of this study is to understand biological responses related to dupilumab treatment among severe asthma patients. Not all asthma is the same, and characteristics of asthma vary from person to person. The study will investigate whether the study drug can help to improve the health of participants lungs, boost immune response, as well as improve quality of life.
Trial arms
Trial start
2022-02-22
Estimated PCD
2023-06-29
Trial end
2023-06-29
Status
Completed
Phase
Early phase I
Treatment
Dupilumab
Participants will receive 8 doses of Dupilumab. The initial loading dose (visit 1) of 600 milligrams (two 300 milligram injections) will be given subcutaneously (SQ). Then the participants will receive 300 milligrams SQ every other week (q 2 weeks) either at a study visit or self-administered at home between visits. Additionally, participants will complete questionnaires, have specimens collected, as well as perform breathing procedures at various timepoints.
Arms:
Dupilumab
Other names:
Dupixent
Size
15
Primary endpoint
Changes in alpha-diversity of respiratory microbiota
Baseline (before dupilumab), 1 month
Changes in alpha-diversity of respiratory microbiota
Baseline (before dupilumab), 4 month
Changes in alpha-diversity of respiratory microbiota
1 month, 4 months
Change in beta-diversity of respiratory microbiota
Baseline (before dupilumab), 1 month
Change in beta-diversity of respiratory microbiota
Baseline (before dupilumab), 4 month
Change in beta-diversity of respiratory microbiota
1 month, 4 months
Change in relative abundances of microbiota members
Baseline (before dupilumab), 1 month
Change in relative abundances of microbiota members
Baseline (before dupilumab), 4 month
Change in relative abundances of microbiota members
1 month, 4 months
Change in respiratory bacterial burden
Baseline (before dupilumab), 1 month
Change in respiratory bacterial burden
Baseline (before dupilumab), 4 month
Change in respiratory bacterial burden
1 month, 4 months
Changes in alpha-diversity of stool microbiota
Baseline (before dupilumab), 1 month
Changes in alpha-diversity of stool microbiota
Baseline (before dupilumab), 4 month
Changes in alpha-diversity of stool microbiota
1 month, 4 months
Change in beta-diversity of stool microbiota
Baseline (before dupilumab), 1 month
Change in beta-diversity of stool microbiota
Baseline (before dupilumab), 4 month
Change in beta-diversity of stool microbiota
1 month, 4 months
Eligibility criteria
Inclusion Criteria: * Physician-diagnosed/managed severe asthma patients that are clinically eligible for dupilumab * Current treatment with a medium-to-high-dose inhaled glucocorticoid (fluticasone propionate at a total daily dose of greater or equal (≥) 440 μg or equipotent equivalent) plus up to at least one additional controller (e.g., a long-acting β2-agonist or leukotriene receptor antagonist) * Eosinophilic asthma phenotype (blood eosinophil level \>300) or asthma requiring daily oral corticosteroids * Asthma that is uncontrolled, as defined by a score on the Asthma Control Test of 19 or lower, or a worsening of asthma in the past year that led to an asthma hospitalization, Emergency Department visit, or 3 days of oral corticosteroids * Severity of asthma that, in the opinion of the subject's asthma care specialist, requires dupilumab for control * For women of childbearing age: agree to use birth control or remain abstinent during the duration of the study. Exclusion Criteria: * Patients with diagnosis of other chronic lung diseases (e.g. Chronic obstructive pulmonary disease (COPD), idiopathic pulmonary fibrosis, Churg-Strauss syndrome, Allergic bronchopulmonary aspergillosis, etc.) * Current smoker or reported smoking within 1 month of the screening visit (tobacco or any inhaled recreational product) * Greater than 10 total pack-year of cigarette smoking history * Treatment with oral corticosteroids for an asthma exacerbation 1 month prior to screening or during the screening period * Use of any biologic therapy for asthma within the past 3 months * Respiratory or Gastrointestinal illness within 1 month prior to screening or during the screening period * Treatment with antibiotics for acute infections within six weeks prior to screening or during the screening period. * Pregnancy at enrollment or during the study * Known hypersensitivity to dupilumab or its excipients
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE4'], 'designInfo': {'allocation': 'NA', 'interventionModel': 'SINGLE_GROUP', 'primaryPurpose': 'BASIC_SCIENCE', 'maskingInfo': {'masking': 'NONE'}}, 'enrollmentInfo': {'count': 15, 'type': 'ACTUAL'}}
Updated at
2023-08-16

1 organization

1 product

1 indication

Product
Dupilumab
Indication
Asthma