This is a phase II study in patients with previously treated immunoglobulin light-chain (AL) Amyloidosis to evaluate the efficacy and safety of teclistamab
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
30
Teclistamab will be administered via a subcutaneous injection
Peking Union Medical College Hospital
Beijing, Beijing Municipality, China
RECRUITINGHematologic complete response (CR) at 3 months after treatment initiation
Time frame: at 3 months after treatment initiation
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