A Real-world Study of Remibrutinib in Chronic Spontaneous Urticaria Patients
Part of paid clinical trials in East Hanover, New Jersey.
- Sponsor
- Novartis Pharmaceuticals
- Study ID
- NCT07408219
- Status
- Recruiting
Conditions
- Chronic Spontaneous Urticaria
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 100 Years
- Healthy Volunteers
- Not accepted
Study Details
This is a United States (US) based, prospective, non-interventional, provider-referral study to evaluate the real-world effectiveness and patient-centered outcomes of remibrutinib in chronic spontaneous urticaria (CSU) patients using validated patient reported outcome (PRO) tools.
Key Dates
- Start date
- Jan 17, 2026
- Status verified
- May 2026
- Primary completion
- Sep 30, 2026
- Completion
- Sep 30, 2026
Study Design
- Enrollment
- 350 participants (estimated)
Arms
- Arm: Remibrutinib CohortAdult patients with CSU who are prescribed and initiating treatment with remibrutinib.
- Arm: Dupilumab CohortAdult patients with CSU who are prescribed and initiating treatment with dupilumab.
Primary Outcome Measure
Change From Baseline in Urticaria Control Test - 7 Day Recall (UCT-7) Score at Week 4 in Patients Initiating Remibrutinib [ Time Frame: Baseline and Week 4 ]
Central Contacts
- Novartis Pharmaceuticals+41613241111
- Novartis Pharmaceuticals
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Novartis | East Hanover | New Jersey | 07936 | - |
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