Dupilumab Effects Against Aeroallergen Challenge

Running, not enrolling · Phase 2 · Has a placebo group

Conditions studied: Asthma, Allergic

In brief

The trial involves two interventions: (i) exposure to HDM in the ACC and (ii) administration of dupilumab/placebo for dupilumab.

Key facts

Study ID

NCT05720325

Run by

The University of Texas Health Science Center at San Antonio

People needed

88

Starts

2023-03-29

Expected to finish

2027-11-01

Last updated by the study team

2026-06-15

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Will demonstrate understanding of the study and will provide a signed and dated informed consent.
• Will be male or female, 18 to 65 years of age at the time of the screening visit.
• Will have symptoms consistent with perennial nasal allergy for a minimum of 2 years prior to the screening visit.
• Will have a positive standard skin prick test (SPT) to D. pteronyssinus within 24 months of screening. A positive SPT is defined as a wheal diameter of at least 5 mm larger than the negative control (normal saline).
• Will have asthma with a documented FEV1 reversibility of ≥10% within 18 months of screening.
• If a participant manifests symptoms suggestive of COVID-19, the participant must have a negative SARS-CoV-2 rapid antigen nasopharyngeal swab test before each HDM exposure visit.
• A woman of childbearing potential, must have a negative urine pregnancy test at Visit 1 and prior to each exposure in the ACC. All women of childbearing potential must agree to a medically acceptable form of birth control throughout the study duration and for at least 2 months prior to Visit 1. Acceptable methods of birth control for this study include:
• oral, patch, or intra-vaginal contraceptives
• Norplant System® or other implant system
• Depo-Provera®
• IUD
• double barrier method
• abstinence
• surgical sterility (hysterectomy, tubal ligation, or uterine ablation)
• Post-menopausal women defined as women without a menstrual cycle for at least 12 consecutive months qualify as non-childbearing for this study.
• Will have never smoked or will be an ex-smoker (<20 pack year history and no cigarette or smokeless tobacco use in the past year).

You may not qualify if…

• Have a chronic lung disease other than asthma.
• Have atopic dermatitis.
• Have any ocular disease that is not associated with allergic rhinoconjunctivitis.
• Are on home oxygen requirement.
• Have a history of rebound nasal congestion (brought on by extended use of topical decongestants), chronic rhinosinusitis with or without nasal polyps, nasal septal perforation, or severe nasal tract malformations noted on physical exam.
• Have FEV1 <70% predicted as determined by pre-bronchodilator spirometry at visit 1.
• Are unwilling/unable to withhold intranasal steroids or asthma medications before specified visits.
• Are unwilling/unable to abstain from protocol-defined prohibited medications for the protocol-specified times before and during screening/selection and ACC HDM exposure visits.
• Have received any oral or other form of systemic glucocorticosteroids within 1 month prior to the screening visit.
• Have received JAK-1 inhibitors within 3 months prior to the screening visit.
• Have known hypersensitivity to dupilumab or any of its excipients.
• Have an ongoing helminth infection.
• Have received a live vaccine within 30 days of screening or are planned to receive one during study participation.Note: Participant can receive a live vaccine > 30 days after final study investigational product injection (visit 14)
• Are pregnant or nursing.
• Have a history of keratoconjunctivitis sicca.
• Have indoor pet exposure causing upper or lower symptoms.
• Have received allergen immunotherapy of any form within 12 months of screening visit.
• Received biologics, other than anti-obesity or diabetes medications (such as tirzepatides, semaglutides), for any indication within 12 months of screening visit.
• Have participated in a trial with an investigational drug in the past 30 days.
• Have past or current medical problems or findings from physical examination or laboratory testing that are not listed above, that, in the opinion of the investigator, may pose additional risks from participation in the study, may interfere with the participant's ability to comply with study requirements, or may impact the quality or interpretation of the data obtained from the study.

Where it is running

• Biogenics Research Chamber — San Antonio, Texas, United States
• University of Texas Health Science Center at San Antonio — San Antonio, Texas, United States

Full record on ClinicalTrials.gov

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