Mechanisms of Dupilumab in AERD
Primary Purpose
Aspirin-exacerbated Respiratory Disease
Status
Not yet recruiting
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
Aspirin Challenge
Sponsored by
About this trial
This is an interventional treatment trial for Aspirin-exacerbated Respiratory Disease
Eligibility Criteria
Inclusion Criteria:
- Subjects >18 years old with Aspirin-Exacerbated Respiratory Disease
This is diagnosed via either a positive oral aspirin or intranasal ketorolac challenge OR a history of at least two stereotypical hypersensitivity reactions to aspirin leading to nasal-ocular symptom and/or asthmatic symptoms.
-All subjects will be required to have a known history of nasal polyposis either via imaging, endoscopy, or nasal examination
Exclusion Criteria:
- History of gastrointestinal reactions (severe abdominal pain with or without vomiting) during NSAID triggered events
- Unstable asthma or history of severe reactions during previous desensitization attempts
- inability to take montelukast pretreatment
- history of gastrointestinal bleeding or bleeding disorder
- pregnancy
- ongoing treatment with an asthma biologic or dupilumab
- previous use of an asthma biologic of dupilumab in the past 3 months
- need for systemic corticosteroids to stabilize asthma prior to challenge
- time from sinus surgery <1 month.
Sites / Locations
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Aspirin Challenge
Arm Description
All subjects will undergo a standardized aspirin challenge
Outcomes
Primary Outcome Measures
Rate of positive challenges to aspirin challenge
Aspirin challenge reactions will be defined as either 1) >15% drop in FEV1 or 2) >25% drop in peak nasal inspiratory flow (PNIF) or 3) >5 point change in composite symptom score.
Spirometry is a standardized measure of airflow obstruction used to define lower airway reaction to aspirin in AERD.
Nasal inspiratory flow rates are measured using an inverted peak flow meter and have been correlated with nasal obstruction occurring during nasal reactions to aspirin in AERD.
Symptom Score - symptoms are a typical part of an aspirin reaction with increase in congestion, itching, cough, and chest tightness.
Secondary Outcome Measures
Full Information
NCT ID
NCT05031455
First Posted
August 19, 2021
Last Updated
February 7, 2023
Sponsor
Scripps Clinic
Collaborators
University of California, San Diego, Regeneron Pharmaceuticals
1. Study Identification
Unique Protocol Identification Number
NCT05031455
Brief Title
Mechanisms of Dupilumab in AERD
Official Title
Mechanisms of Dupilumab in AERD - Effects on Aspirin Hypersensitivity Response, With a Focus on Innate Type 2 Inflammatory Responses
Study Type
Interventional
2. Study Status
Record Verification Date
February 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
May 31, 2023 (Anticipated)
Primary Completion Date
December 31, 2025 (Anticipated)
Study Completion Date
February 28, 2026 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Scripps Clinic
Collaborators
University of California, San Diego, Regeneron Pharmaceuticals
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
No
5. Study Description
Brief Summary
Aspirin-Exacerbated Respiratory Disease (AERD), although uncommon in the general population, is an important phenotype of severe asthma and nasal polyposis where it occurs in 15% of severe asthmatics, and up to 30% of those with nasal polyposis. An important therapy for AERD is aspirin therapy after desensitization (ADAT). This is an inexpensive and proven therapy to improve the burden of sinus disease in AERD. Aspirin desensitization is the mechanism by which tolerance is induced in AERD patients. This is a 1-2 day outpatient procedure whereby increasing doses of aspirin are administered and the patients invariably experience some degree of hypersensitivity reactions.
It is important to understand the effect of medications on the aspirin desensitization. It is known that the leukotriene modifier medications decrease the severity of the reactions in AERD. Other treatments such as antihistamines and the biologic agent omalizumab might have an effect on either blocking or blunting reactivity in AERD during desensitization.
Dupilumab is a new respiratory biologic approved for atopic dermatitis, eosinophilic asthma and nasal polyposis. As such, it is well situated to be used for many AERD patients whose disease cannot be well controlled. The effect of dupilumab on the aspirin desensitization process and reaction is unknown and is the topic of this investigation.
The primary objective is to determine the effect of dupilumab on reactions during aspirin challenge/desensitization.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Aspirin-exacerbated Respiratory Disease
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
16 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Aspirin Challenge
Arm Type
Experimental
Arm Description
All subjects will undergo a standardized aspirin challenge
Intervention Type
Drug
Intervention Name(s)
Aspirin Challenge
Other Intervention Name(s)
Dupixent
Intervention Description
Dupilumab is a fully human monoclonal antibody that blocks the receptor component for IL-4 and IL-13, which are key drivers of type 2 inflammation. All subjects will be prescribed this at standard 300mg subcutaneous dosing every 2 weeks. The intervention will be the response to aspirin challenge.
8 of 16 subjects will randomly receive dupilumab. All subjects will undergo an aspirin challenge/desensitization procedure. To achieve adequate steady state levels of dupilumab, the dosing regimen will be a 600mg loading dose of dupilumab followed by 300mg subcutaneous at 1 week, 3 weeks and 5 weeks. Aspirin challenge/desensitization will take place at week 6 after dupilumab loading dose.
Primary Outcome Measure Information:
Title
Rate of positive challenges to aspirin challenge
Description
Aspirin challenge reactions will be defined as either 1) >15% drop in FEV1 or 2) >25% drop in peak nasal inspiratory flow (PNIF) or 3) >5 point change in composite symptom score.
Spirometry is a standardized measure of airflow obstruction used to define lower airway reaction to aspirin in AERD.
Nasal inspiratory flow rates are measured using an inverted peak flow meter and have been correlated with nasal obstruction occurring during nasal reactions to aspirin in AERD.
Symptom Score - symptoms are a typical part of an aspirin reaction with increase in congestion, itching, cough, and chest tightness.
Time Frame
Aspirin challenge = 6 weeks after starting dupilumab/placebo. Aspirin challenge day = up to 8 hours
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Subjects >18 years old with Aspirin-Exacerbated Respiratory Disease
This is diagnosed via either a positive oral aspirin or intranasal ketorolac challenge OR a history of at least two stereotypical hypersensitivity reactions to aspirin leading to nasal-ocular symptom and/or asthmatic symptoms.
Current treatment with dupilumab at standard asthma/nasal polyposis dosing of 300mg subcutaneously every 2 weeks for a minimum of 12 weeks.
All subjects will be required to have a known history of nasal polyposis either via imaging, endoscopy, or nasal examination
Exclusion Criteria:
History of gastrointestinal reactions (severe abdominal pain with or without vomiting) during NSAID triggered events
Unstable asthma or history of severe reactions during previous desensitization attempts
inability to take montelukast pretreatment
history of gastrointestinal bleeding or bleeding disorder
pregnancy
previous use of any other respiratory biologic in the past 3 months (omalizumab, tezepelumab, mepolizumab, reslizumab, benralizumab)
need for systemic corticosteroids to stabilize asthma prior to challenge
time from sinus surgery <1 month.
12. IPD Sharing Statement
Learn more about this trial
Mechanisms of Dupilumab in AERD
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