This is a prospective, single-arm clinical study designed to evaluate the efficacy and safety of the BCMA/CD3 bispecific antibody (CM336) as maintenance therapy after autologous hematopoietic stem cell transplantation in patients with newly diagnosed multiple myeloma.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
20
Anti-BCMA/CD3 bispecific antibody (CM336) will be administered via a subcutaneous injection (SC).
Institute of Hematology and Blood Diseases Hospital Chinese Academy of Medical Sciences
Tianjin, China
RECRUITINGMinimal residual disease (MRD) negativity conversion rate
Time frame: Up to 24 months
Duration of MRD negativity
Time frame: Up to 24 months
Progression-Free Survival
Time frame: From enrollment to the date of disease progression or death, up to approximately 24 months.
Overall Survival (OS)
Time frame: From start of treatment until death from any caus, up to approximately 24 months.
Incidence and severity of adverse events (AEs)
Time frame: From the first dose through 30 days after the last dose, up to approximately 24 months.
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