Effects of Interleukin (IL)- 4R-alpha Inhibition on Respiratory Microbiome and Immunologic Correlates in Severe Asthma

Asthma Clinical Trial

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05036733
• Other study ID #: HUM00196809
• Status: Completed
• Phase: Phase 4
• Start date: February 22, 2022
• Est. completion date: June 29, 2023

Study information

• Verified date: August 2023
• Source: University of Michigan
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 15
• Est. completion date: June 29, 2023
• Est. primary completion date: June 29, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

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 ß2-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

Related Conditions & MeSH terms

• Asthma

Intervention

Drug:
• 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.

Locations

Country	Name	City	State
United States	University of Michigan	Ann Arbor	Michigan

Sponsors (2)

Lead Sponsor	Collaborator
University of Michigan	Regeneron Pharmaceuticals

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Changes in alpha-diversity of respiratory microbiota	This will be profiled from induced sputum.	Baseline (before dupilumab), 1 month
Primary	Changes in alpha-diversity of respiratory microbiota	This will be profiled from induced sputum.	Baseline (before dupilumab), 4 month
Primary	Changes in alpha-diversity of respiratory microbiota	This will be profiled from induced sputum.	1 month, 4 months
Primary	Change in beta-diversity of respiratory microbiota	This will be profiled from induced sputum.	Baseline (before dupilumab), 1 month
Primary	Change in beta-diversity of respiratory microbiota	This will be profiled from induced sputum.	Baseline (before dupilumab), 4 month
Primary	Change in beta-diversity of respiratory microbiota	This will be profiled from induced sputum.	1 month, 4 months
Primary	Change in relative abundances of microbiota members	This will be profiled from induced sputum.	Baseline (before dupilumab), 1 month
Primary	Change in relative abundances of microbiota members	This will be profiled from induced sputum.	Baseline (before dupilumab), 4 month
Primary	Change in relative abundances of microbiota members	This will be profiled from induced sputum.	1 month, 4 months
Primary	Change in respiratory bacterial burden	This will be profiled from induced sputum.	Baseline (before dupilumab), 1 month
Primary	Change in respiratory bacterial burden	This will be profiled from induced sputum.	Baseline (before dupilumab), 4 month
Primary	Change in respiratory bacterial burden	This will be profiled from induced sputum.	1 month, 4 months
Primary	Changes in alpha-diversity of stool microbiota	This will be based on stool samples.	Baseline (before dupilumab), 1 month
Primary	Changes in alpha-diversity of stool microbiota	This will be based on stool samples.	Baseline (before dupilumab), 4 month
Primary	Changes in alpha-diversity of stool microbiota	This will be based on stool samples.	1 month, 4 months
Primary	Change in beta-diversity of stool microbiota	This will be based on stool samples.	Baseline (before dupilumab), 1 month
Primary	Change in beta-diversity of stool microbiota	This will be based on stool samples.	Baseline (before dupilumab), 4 month
Primary	Change in beta-diversity of stool microbiota	This will be based on stool samples.	1 month, 4 months
Secondary	Forced expiratory volume ( FEV1) / forced vital capacity (FVC) ratio	This will be based on Spirometry	up to 4 months
Secondary	Forced expiratory volume (FEV1)	This will be based on Spirometry	up to 4 months
Secondary	Change in Fractional exhaled nitric oxide (FeNO)		Baseline, 4 months
Secondary	Asthma Control Test (ACT)	This is a self-administered 5 item questionnaire. The ACT score is the sum of the values for all 5 items. The scores range from 5 (poor control of asthma) to 25 (complete control of asthma), with higher scores reflecting greater asthma control. An ACT score >19 indicates well-controlled asthma; the minimal clinically important difference in score is 3.	up to 4 months
Secondary	Mini Asthma Quality of Life Questionnaire Score (mAQLQ)	This is a patient self-administered questionnaire with 15 questions covering 4 domains: Symptoms (5 questions), Activity Limitations (4 questions), Emotional Function (3 questions), and Environmental Stimuli (3 questions). Scores range from 0-6 (lower is worse). The mini AQLQ score is calculated as the average of domain items. The minimum clinically important difference is 0.5.; Overall score (average of 15 questions): add up responses to all questions, and divide by 15.	up to 4 months
Secondary	Sino-nasal outcome test (SNOT-22)	This is a 22 item questionnaire. Each item is rated as follows: 0=no problem, 1=very mild problem, 2=mild or slight problem, 3=moderate problem, 4=severe problem, 5=problem as bad as it can be. The score ranges between 0 and 110. A higher score means worse outcome.	up to 4 months
Secondary	Change in prescribed maintenance corticosteroid use (inhaled or oral), between baseline and 4 months.		Baseline, 4 months
Secondary	Number of asthma exacerbations requiring at least 3 days of oral corticosteroids		up to 4 months