RecruitingNCT07408219

A Real-world Study of Remibrutinib in Chronic Spontaneous Urticaria Patients

RELIEF: Remibrutinib in Chronic Spontaneous Urticaria: Early Real World Effectiveness and Satisfaction Survey

Sponsor

Novartis Pharmaceuticals

Enrollment

350 participants

Start Date

Jan 17, 2026

Study Type

OBSERVATIONAL

Conditions

Chronic Spontaneous Urticaria

Summary

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.

Eligibility

Min Age: 18 YearsMax Age: 100 Years

Inclusion Criteria4

Healthcare provider (HCP) participants eligible to refer patients for inclusion in this study must meet all the following criteria:
Have an active medical license and be board certified/board eligible allergist or dermatologist in the US. Nurse practitioners and physician assistant practicing in allergy and dermatology are eligible.
Manage CSU patients within their practice.
Enrolled in the research network or are referred HCPs who agree to participate.

Exclusion Criteria13

Patients eligible for inclusion in this study must meet all of the following criteria:
≥ 18 years of age.
Diagnosed with CSU by an HCP.
Have received a prescription for remibrutinib or dupilumab and are expected to initiate treatment.
Have access to an electronic device with internet capabilities.
Able to read and understand English.
Willing and able to provide consent for study participation.
Patients will be excluded if they meet any of the following criteria:
Unable to procure remibrutinib or dupilumab (through samples, commercially or patient assistance program).
Exposure to oral corticosteroid treatment in 14 days prior to consent.
Exposure to oral corticosteroid treatment in 14 days prior to initiating treatment with remibrutinib or dupilumab.
Prior participation in a remibrutinib or dupilumab clinical trial.
Cognitive impairment that impacts the patient's ability to participate.