This clinical trial is a multicenter, randomized, double-blind, controlled phase III clinical study.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
420
VC005 groups repeat administration for 48 weeks
VC005 placebo groups repeat administration for 48 weeks
Peking University People's Hospital
Beijing, Beijing Municipality, China
RECRUITINGPercentage of patients achieving an Assessment of disease activity (signs and symptoms) in ankylosing spondylitis 20% improvement (ASAS20) in response at week 12 of treatment.
Time frame: week 12
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