This is a open-label, multi-center study to evaluate the safety and efficacy of CM326 in atopic adrmatitis subjects.
The study consists of 3 periods, a up-to-4-week Screening Period, a 52-week Treatment Period and a 8-week Safety Follow-up Period.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
100
CM326 injection
Peking University People's hospital
Beijing, China
RECRUITINGIncidence of treatment-emergent adverse events
Incidence of treatment-emergent Adverse events related to CM326
Time frame: at week 52
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