This is a multi-center, single arm, open-label study to evaluate safety and primary efficacy in children patients with moderate-to severe atopic dermatis.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
24
CM310 600 mg + 300 mg, subcutaneous injection
Beijing Children's Hospital Capital Medical University
Beijing, China
Adverse events
Incidence of adverse events.
Time frame: at week 14
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