This is an open-label, single-arm, multicenter, expansion study to evaluate the safety and efficacy of CM512 in patients With Chronic Rhinosinusitis with Nasal Polyposis
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
120
Administered subcutaneous injection
Beijing Tong-Ren hospital
Beijing, China
Occurrence of adverse events
Incidences of adverse events
Time frame: Up to week 64
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