A Study to Evaluate the Long Term Safety and Efficacy of Bimekizumab in Subjects With Ankylosing Spondylitis
Part of paid clinical trials in Sarasota, Florida.
- Sponsor
- UCB Biopharma SRL
- Study ID
- NCT03355573
- Phase
- PHASE2
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Bimekizumab — DRUGBimekizumab at a prespecified dose.
Study Details
This is a study to assess the long term safety and tolerability of bimekizumab in subjects with ankylosing spondylitis
Key Dates
- Start date
- Nov 28, 2017
- Status verified
- Nov 2024
- Primary completion
- Oct 19, 2022
- Completion
- Oct 19, 2022
Study Design
- Enrollment
- 255 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: BimekizumabSubjects will receive bimekizumab up to 4 years.
Primary Outcome Measure
Percentage of Participants With Treatment-emergent Adverse Events (TEAEs) During the Study [ Time Frame: From Entry Visit (Visit 1) until Safety Follow Up (up to Week 224) ]
Locations (3)
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