Drug intelligence / Profile preview

trastuzumab deruxtecan + volrustomig

Development stage
Unknown
Lead developer
Daiichi Sankyo
Modality
Bispecific Antibodies → Multispecific Antibodies → Engineered Antibody Formats → Antibody-Based Therapeutics, Cytotoxic ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

**Trastuzumab deruxtecan + volrustomig** is an investigational combination therapy composed of two distinct drugs: - **Trastuzumab deruxtecan (T-DXd)** is an antibody-drug conjugate (ADC) targeting the human epidermal growth factor receptor 2 (HER2). The antibody specifically binds HER2, and is conjugated to a cytotoxic topoisomerase I inhibitor (deruxtecan) via a cleavable linker. Upon binding HER2-expressing tumor cells, it is internalized and the cytotoxic payload is released to induce cell death. - **Volrustomig (MEDI5752)** is a bispecific monoclonal antibody that simultaneously targets the programmed cell death protein 1 (PD-1) and cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4), promoting immune activation by blocking inhibitory checkpoint pathways. The combination is being investigated as a treatment in HER2-positive cancers (notably gastric, esophageal, and non-small cell lung cancers), leveraging both direct cytotoxicity and immune-mediated antitumor response[1][2][4].

Other names
T-DXdtrastuzumab deruxtecanvolrustomigMEDI5752MEDI-5752MEDI 5752
02

Targets

TOP1 (DNA Topoisomerase I)PDCD1 (Programmed cell death protein 1 receptor)ERBB2 (Erb-b2 receptor tyrosine kinase 2)CTLA-4 (Cytotoxic t-lymphocyte–associated protein 4)

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