The purpose of this study is to assess the safety, tolerability, PK, PD, immunogenicity, and preliminary clinical activity of cizutamig in patients with IgAN.
An Open-Label Study Evaluating the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, Immunogenicity, and Preliminary Clinical Activity of Cizutamig in Patients with Immunoglobulin A Nephropathy
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
15
Cizutamig will be dosed according to the protocol.
Peking University First Hospital
Beijing, China
Number of participants with treatment-related adverse events as assessed by CTCAE v5.0
Incidence and severity of TEAEs through end of study: 1. Incidence and severity of treatment-emergent adverse events through end of study 2. Changes from baseline in vital signs, ECG, and laboratory assessments through end of study
Time frame: Baseline up to 52 weeks
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