Study of Inhaled ARO-RAGE in Allergen-induced Mild Asthma
Recruiting now · Phase 2 · Has a placebo group
Conditions studied: Asthma
In brief
The purpose of this study is to evaluate the impact of inhaled ARO-RAGE on the late asthmatic response (LAR) following an inhaled allergen challenge in participants with mild atopic asthma.
Key facts
- Study ID
- NCT07241546
- Run by
- Arrowhead Pharmaceuticals
- People needed
- 36
- Starts
- 2026-03-30
- Expected to finish
- 2028-04-01
- Last updated by the study team
- 2026-06-23
Who can join
Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Clinically stable, mild atopic asthma (FEV1 ≥70% predicted)
- Established allergy confirmed by positive skin prick test at screening
- Willing and able to perform lung function tests and other study-related procedures
- Participants of childbearing potential must consent to use a method of highly-effective contraception in addition to a condom during the study and for at least 90 days following the end of study or last investigational product administration, whichever is later
You may not qualify if…
- Concomitant diagnosis of a clinically important pulmonary disease other than asthma
- Use of corticosteroids, immunosuppressives, or anti-inflammatory medications that interfere with inhaled challenges or inflammation, or chronic use of any other medication for treatment of allergic asthma
- History or current medical condition contraindicating methacholine challenge
- Note: Additional inclusion/exclusion criteria may apply per protocol.
Where it is running
- Research Site 1 — Vancouver, British Columbia, Canada (enrolling)
- Research Site 2 — Calgary, Canada (enrolling)
- Research Site 3 — Edmonton, Canada (enrolling)
- Research Site 5 — Hamilton, Canada (enrolling)
- Research Site 4 — Saskatoon, Canada (enrolling)
Full record on ClinicalTrials.gov
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