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acapatamab + enzalutamide
- Development stage
- Unknown
- Lead developer
- Amgen
- Modality
- Bispecific Antibodies → Multispecific Antibodies → Engineered Antibody Formats → Antibody-Based Therapeutics, Small Molecules
- Administration
- Intravenous, Oral
01
Overview
This is a **combination therapy** consisting of acapatamab, a half-life extended bispecific monoclonal antibody that targets prostate-specific membrane antigen (PSMA) on prostate cancer cells and CD3 on T cells, and enzalutamide, an androgen receptor inhibitor. Acapatamab acts as a T-cell engager to direct immune-mediated killing of prostate cancer cells, while enzalutamide inhibits androgen signaling that drives prostate cancer progression. Acapatamab is being developed and studied primarily for metastatic castration-resistant prostate cancer (mCRPC), particularly in patients refractory to androgen receptor pathway inhibitor therapy and taxane-based chemotherapy. The combination is under evaluation to potentiate antitumor immune activity and androgen deprivation[5].
- Other names
- PSMA × CD3 bispecific T-cell engager + enzalutamideacapatamab + enzalutamide
02
Targets
CD3 (T-cell surface glycoprotein CD3)PSMA (Prostate-specific membrane antigen)AR (Adrenergic receptors)
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