Rozanolixizumab for Myasthenia Gravis
(MyVisionXT Trial)
What You Need to Know Before You Apply
What is the purpose of this trial?
The purpose of the study is to assess the long-term safety and efficacy of rozanolixizumab in adult study participants with ocular myasthenia gravis.
Are You a Good Fit for This Trial?
This trial is for adults with ocular myasthenia gravis who have already received at least one dose of rozanolixizumab or placebo in a previous study. Participants must be able to follow the study schedule and, if female and able to become pregnant, agree to use contraception.Inclusion Criteria
Exclusion Criteria
What Are the Treatments Tested in This Trial?
Interventions
- Rozanolixizumab
Trial Overview
The study is testing the long-term safety and effectiveness of rozanolixizumab in people with ocular myasthenia gravis. All participants will receive this medication over an extended period.
How Is the Trial Designed?
1
Treatment groups
Experimental Treatment
The study is composed of Extended Observation Period(s) and Symptom-driven Cycle(s). Based on their clinical need for treatment, study participants will be able to start the study with either an Extended Observation Period or a Symptom-driven Cycle. A Symptom-driven Cycle will be initiated based on disease worsening and participants will receive rozanolixizumab based on investigator's medical judgement.
Find a Clinic Near You
Who Is Running the Clinical Trial?
UCB Biopharma SRL
Lead Sponsor
Jean-Christophe Tellier
UCB Biopharma SRL
Chief Executive Officer since 2015
MD from University of Reims Champagne-Ardenne, Rheumatology specialization from University of Paris V, Executive business programs at Harvard and INSEAD
Dr. Iris Loew-Friedrich
UCB Biopharma SRL
Chief Medical Officer since 2014
MD from University of Leuven, PhD in Medical Sciences from University of Leuven
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