This study is a multi-center, randomized, double-blind, parallel controlled phase 2 study, aimed at evaluating the efficacy and safety of CM310 in the treatment of patients with moderate-to-severe atopic dermatitis, and observing Pharmacokinetics characteristics, Pharmacodynamics effects and immunogenicity.
This study includes screening, treatment and follow-up periods. 160 subjects will be enrolled to receive CM310.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
160
IL-4Rα monoclonal antibody
Hangzhou First People's Hospital
Hangzhou, Zhejiang, China
Proportion of subjects achieving EASI-75
Proportion of subjects achieving EASI-75 (≥75% reduction from baseline in Eczema Area and Severity Index score).
Time frame: up to week 12
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