Mechanisms of Benefit of IL4RA Inhibition in Aspirin-Exacerbated Respiratory Disease

Description

The overall aim of the study is to determine the clinical efficacy and mechanisms of action of anti-IL-4a (dupilumab) as treatment for patients with Aspirin-Exacerbated Respiratory Disease (AERD).

Conditions

Nasal Polyps, Asthma, Aspirin-Induced, Aspirin-Exacerbated Respiratory Disease, Aspirin-Sensitive Asthma With Nasal Polyps

Study Overview

Study Details

Study overview

The overall aim of the study is to determine the clinical efficacy and mechanisms of action of anti-IL-4a (dupilumab) as treatment for patients with Aspirin-Exacerbated Respiratory Disease (AERD).

Mechanisms of Benefit of IL4RA Inhibition in Aspirin-Exacerbated Respiratory Disease: MARINER

Mechanisms of Benefit of IL4RA Inhibition in Aspirin-Exacerbated Respiratory Disease

Condition
Nasal Polyps
Intervention / Treatment

-

Contacts and Locations

Boston

Brigham and Women's Hospital, Boston, Massachusetts, United States, 02115

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • 1. History of AERD, defined as meeting the diagnostic triad with:
  • 1. History of physician-diagnosed asthma and
  • 2. History of physician-diagnosed nasal polyposis and
  • 3. History of pathognomonic reactions to aspirin or other nonselective COX inhibitors.
  • 2. Visible nasal polyps bilaterally on otoscope physical exam at the time of screening.
  • 3. Evidence of sense of smell impairment, with a University of Pennsylvania Smell Identification Test (UPSIT) score of \<34.
  • 4. Stable asthma (no glucocorticoid burst for at least 4 weeks prior to Visit 1, and no hospitalizations or ER visits for asthma for at least the prior 3 months).
  • 5. Consistent (daily) use of an intranasal steroid for at least 4 weeks prior to Screening.
  • 6. No current smoking (not more than one instance of smoking in the last 3 months).
  • 7. For females: Practicing FDA-approved methods of birth control for the duration of the study. Female participants of childbearing potential must have a negative pregnancy test upon study entry.
  • 1. Use of investigational drugs within 12 weeks of Screening.
  • 2. Use of any biologic agent within 4 months prior to Screening.
  • 3. Use of systemic (enteral or injected) glucocorticoids within 4 weeks prior to Screening.
  • 4. History of any sinonasal surgery within 4 months prior to Screening
  • 5. Current use of zileuton
  • 6. Current use of high-dose aspirin therapy (no more than 325 mg aspirin per day will be allowed)
  • 7. Pregnant, nursing, or planning to become pregnant

Ages Eligible for Study

18 Years to 70 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Brigham and Women's Hospital,

Tanya M Laidlaw, MD, PRINCIPAL_INVESTIGATOR, Brigham and Women's Hospital

Study Record Dates

2026-04-30