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Viral Infection in Asthma (VIA) Study

Study acronym: VIA
StatusRecruiting
PhasePhase 4
Started
View on ClinicalTrials.gov ↗
Record status
This record was last updated April 1, 2025 (before its estimated June 30, 2026 completion). Its status may not reflect the trial's current state.

Record History

See every version on ClinicalTrials.gov ↗

  1. Notable Primary completion date: May 31, 2025 to Jun 30, 2026
    • Study completion date: Jan 31, 2026 to Dec 31, 2026
    v6
  2. Notable Primary completion date: May 31, 2024 to May 31, 2025
    • Study completion date: Jan 31, 2025 to Jan 31, 2026
    • Eligibility criteria expanded, about 2 words
    v5
  3. Notable Trial status: Not Yet Recruiting to Recruitingv4 Show 4 more changesShow less
    • Study sites: 0 to 1
    • Primary completion date: Jan 31, 2024 to May 31, 2024
    • Study completion date: Jan 31, 2024 to Jan 31, 2025
    • Start date changed from estimate of Feb 1, 2022 to May 1, 2022
  4. Notable Start date: Sep 1, 2021 to Feb 1, 2022
    • Primary and study completion dates: Dec 31, 2023 to Jan 31, 2024
    v3
  5. Notable Primary and study completion dates: Jul 30, 2022 to Dec 31, 2023
    • Start date: Jul 30, 2020 to Sep 1, 2021
    v2
  6. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
956 trials monitored
See 34 trials at risk
Often when people with asthma get a virus caused by the common cold (rhinovirus), they also experience an increase or worsening of their asthma symptoms. The purpose of this study is to see if the study medication dupilumab helps prevent those with mild to moderate asthma from having increased asthma symptoms, after being exposed to an experimental rhinovirus inoculation. This is a study about dupilumab which is a drug approved by the U.S. Food and Drug Administration (FDA) for treatment of moderate to severe asthma. Dupilumab is a medication that blocks pathways that cause asthmatic inflammation in the lungs, leading to symptoms and worsening lung function. During this study, subjects will be given either dupilumab or placebo and will subsequently be exposed to the the "common" cold virus (rhinovirus). The virus that the investigators are using has been safely used before in many studies like this involving thousands of volunteers, and the safe use of the virus in this research study has been reviewed by the FDA. The investigators will track asthma symptoms during the study with lung function tests, questionnaires, specimen collection, biomarkers, and physical exams. For data analysis the investigators will assess the samples collected to determine changes in the treatment groups. The investigators will also asses the symptom scores and deviations from baseline measures for lung function.
Trial Details
NCT Number NCT04380038
Lead Sponsor University of Virginia
Collaborators: Regeneron Pharmaceuticals
Conditions
(from sponsor)
Asthma
Related terms Asthma
Enrollment 60 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov