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Not Yet RecruitingNCT06770088

Vunakizumab in Adults with Spondyloarthritis

A Prospective, Single-arm, Multicenter Study to Explore the Efficacy and Safety of Vunakizumab in Adults with Active Spondyloarthritis

Status
Not Yet Recruiting
Phase
Phase 4
Study type
Interventional
Enrollment
880 (estimated)
Sponsor
Sun Yat-sen University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This prospective, single-arm, multicenter study is aimed to explore the efficacy and safety of Vunakizumab in adults with spondyloarthritis. The primary endpoint is the proportion of adults with spondyloarthritis achieving ankylosing spondylitis assessment score (ASAS) 40 at week 16 in the treatment of Vunakizumab.

Conditions

Interventions

TypeNameDescription
DRUGvnacicizumabVunakizumab 120 mg subcutaneous injection at baseline and week2, week4, then every other 4 weeks.

Timeline

Start date
2025-01-10
Primary completion
2026-01-10
Completion
2027-12-31
First posted
2025-01-13
Last updated
2025-01-13

Source: ClinicalTrials.gov record NCT06770088. Inclusion in this directory is not an endorsement.

Vunakizumab in Adults with Spondyloarthritis (NCT06770088) · Clinical Trials Directory