Vilamakitug in Spondyloarthritis Placebo-controlled Investigation for Efficacy
- Sponsor
- XBiotech, Inc.
- Study ID
- NCT06526377
- Phase
- PHASE2
- Status
- Not Yet Recruiting
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Conditions
- Ankylosing Spondylitis
- Axial Spondyloarthritis
- Nr-axSpA
- r-axSpA
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 65 Years
- Healthy Volunteers
- Not accepted
Interventions
- vilamakitug — DRUGVilamakitug is a monoclonal antibody preparation, indistinguishable from a natural antibody isolated from a healthy human.
- placebo — DRUGplacebo
Study Details
The goal of this clinical trial is to find out if the study drug will work as a new therapy for axSpA patients. This study is placebo-controlled, and evaluates if study drug can treat symptoms of axSpA, including global disease activity, pain, function and inflammation.
Key Dates
- Start date
- Sep 30, 2026
- Status verified
- May 2026
- Primary completion
- Sep 30, 2028
- Completion
- Sep 30, 2028
Study Design
- Enrollment
- 150 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: vilamakitugweekly dose of vilamakitug
- Placebo Comparator: placeboplacebo
Primary Outcome Measure
Percentage of participants achieving ASAS40. [ Time Frame: Baseline to week 16 ]
Central Contacts
- XBiotech Clinical(512) 386-2900
- XBiotech Clinical512.386.2900
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