A Study Evaluating the Real World Experience of Participants Treated With BRIUMVI® (Ublituximab-xiiy) for Relapsing Multiple Sclerosis (RMS)
NCT06433752 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 2000
Last updated 2026-05-15
Summary
The purpose of this study is to evaluate safety, effiectiveness, and to gain insight into the treatment experience of participants prescribed BRIUMVI® (ublituximab-xiiy) in the real-world setting
Conditions
Interventions
- OTHER
-
No Intervention
No Intervention
Sponsors & Collaborators
-
TG Therapeutics, Inc.
lead INDUSTRY
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2024-07-22
- Primary Completion
- 2032-04-01
- Completion
- 2032-04-01
- FDA Drug
- Yes
Countries
- United States
- Puerto Rico
Study Locations
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