Drug intelligence / Profile preview

F182112 + CD38

Development stage
Unknown
Lead developer
Shandong New Time Pharmaceutical
Modality
Bispecific Antibodies → Multispecific Antibodies → Engineered Antibody Formats → Antibody-Based Therapeutics, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

F182112 + CD38 is an investigational combination therapy being evaluated for the treatment of relapsed or refractory multiple myeloma (RRMM). F182112 is a humanized bispecific antibody developed by Shandong New Time Pharmaceutical (a subsidiary of Lunan Pharmaceutical Group) that targets B-cell maturation antigen (BCMA) on myeloma cells and the CD3 epsilon subunit on T cells, thereby facilitating T-cell mediated cytotoxicity against tumor cells. The combination regimen involves the administration of F182112 alongside a CD38-targeting monoclonal antibody (such as daratumumab). This dual-antigen targeting approach (BCMA and CD38) is intended to enhance anti-tumor efficacy and overcome resistance in patients who have previously failed standard-of-care treatments, including proteasome inhibitors and immunomodulatory drugs (IMiDs). The regimen is currently being studied in Phase II clinical trials (e.g., NCT07312188).

Other names
F182112 plus CD38 antibodyF-182112 plus CD38 antibodyF 182112 plus CD38 antibodyF182112 and CD38 antibodyF-182112 and CD38 antibodyF 182112 and CD38 antibody
02

Targets

CD3 (T-cell surface glycoprotein CD3)CD38 (Cluster of Differentiation 38)BCMA (B-cell maturation antigen)

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