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🏛️ Verified NIH Protocol • Sourced via U.S. National Library of Medicine (Last Synced: 2026-03-04)

A Study Assessing the Effect of Dupilumab on Inducing Clinical Remission in Asthma

🟢 Recruiting Phase 3 💊 Investigational Drug / Biologic Sponsor: Université de Sherbrooke

🩺 Protocol Summary

This study tests whether an asthma medication called dupilumab can help people achieve complete asthma control (called "remission") when given earlier in their disease, before asthma becomes severe. Currently, most people with asthma only receive advanced treatments like biologics after their condition has worsened significantly and caused lung damage. This study explores whether treating high-risk patients earlier could prevent asthma attacks and lung function decline, potentially achieving remission before permanent damage occurs. The study is looking for adults aged 18-79 with moderate asthma who have had at least one asthma attack requiring steroid pills in the past 2 years, use medium or high-dose inhaled steroids regularly, have high levels of inflammation markers in their blood and breath tests, but don't yet meet criteria for severe asthma requiring biologic therapy. Participants receive either dupilumab or placebo injections every 2 weeks for one year, alongside their regular asthma medications. They attend clinic visits every 3 months for breathing tests, questionnaires, and safety monitoring. Neither participants nor doctors know who receives the real medication until the study ends. The goal is to learn whether early treatment with dupilumab helps more people achieve complete asthma control compared to standard care alone, potentially changing how asthma is treated from "waiting until severe" to "preventing severe disease." The study runs in Canada, the United Kingdom, and Australia, involving 150 participants

Primary Research Facility: Sir Charles Gairdner Hospital (Nedlands, Western Australia)

📋 Basic Study Criteria & Logistics Checklist

0 of 3 Checked

Review these 3 basic logistical and protocol criteria extracted from the public NIH record. (This is a preliminary logistical checklist, not an official clinical eligibility determination).

📍 Primary Site Map

Site: Sir Charles Gairdner Hospital — Nedlands, Western Australia

📍 All Participating Trial Locations (5 Sites)

Multi-Center Trial

This protocol is enrolling participants across multiple clinical centers:

1. Sir Charles Gairdner HospitalNedlands, Western Australia • Contact: 61 8 6488 6000
2. McGill University Health CentreMontreal, Quebec • Contact: (514) 934-1934
3. Institut universitaire de cardiologie et de pneumologie de QuébecQuébec, Quebec • Contact: (418) 656-8711
4. CIUSSS de l'Estrie- CHUSSherbrooke, Quebec • Contact: (819) 346-1110
5. Oxford University Hospitals NHS Foundation Trust - John Radcliffe HospitalOxford, Oxfordshire • Contact: +44 300 304 7777

📄 Print Doctor Discussion Sheet

Preview and print a 1-page summary with 5 tailored questions for your physician.

💰 Clinical Trial Costs & Insurance Coverage

Coverage for clinical trial participation varies depending on your health insurance policy, state legislation, and whether specific procedures are investigational research or routine medical care. Under federal law (Affordable Care Act § 2709), health insurers generally cannot drop coverage or refuse to pay for routine patient care costs incurred in approved clinical trials.

💡 Always ask the study coordinator for the trial's official Informed Consent Form, which outlines all sponsor-funded research items versus procedures billed to your insurance.

🏛️ Official Government Provenance

NIH ClinicalTrials.gov Protocol Record

NCT Identifier: NCT07309614 • Last Synced: 2026-03-04
View on ClinicalTrials.gov ↗
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