Drug intelligence / Profile preview

docetaxel + BMS-986218

Development stage
Unknown
Lead developer
Bristol Myers Squibb
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Intravenous
01

Overview

**docetaxel + BMS-986218** is an investigational combination therapy for advanced or metastatic solid tumors, specifically being studied in metastatic castration-resistant prostate cancer (mCRPC). Docetaxel is a standard chemotherapy agent that acts as a microtubule inhibitor, disrupting cell division. BMS-986218 is a next-generation, non-fucosylated monoclonal antibody targeting cytotoxic T-lymphocyte-associated antigen 4 (CTLA4), designed to enhance immune-mediated anti-tumor effects through checkpoint inhibition and increased antibody-dependent cell cytotoxicity. The primary rationale for the combination is to pair the cytotoxic effect of docetaxel with the immune-stimulatory (checkpoint blockade) actions of BMS-986218 in enhancing anti-tumor responses. This combination is being developed and studied by Bristol Myers Squibb in multi-center clinical trials, and neither agent in this exact combination is currently approved for this indication[1][3][5][6].

02

Targets

CTLA-4 (Cytotoxic t-lymphocyte–associated protein 4)TUBB (Tubulin (alpha and beta subunits))

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