Drug intelligence / Profile preview

mAb104 + monomethyl auristatin E

Development stage
Preclinical
Modality
Small Molecules, Cytotoxic ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

**mAb104 + monomethyl auristatin E** is an experimental antibody-drug conjugate (ADC) comprising the monoclonal antibody mAb104 linked to the synthetic antimitotic agent monomethyl auristatin E (MMAE)[1][4][7]. mAb104 targets a conformationally exposed epitope on HER2 (human epidermal growth factor receptor 2), showing efficacy in HER2-overexpressing cancer xenograft models[3]. MMAE inhibits cell division by blocking tubulin polymerisation and is used as a cytotoxic payload in ADCs for targeted cancer therapy[1][4]. Upon intravenous administration, mAb104 binds to HER2 on cancer cells, is internalized, and MMAE is released (typically via a protease-cleavable linker such as MC-VC-PABC)[4][5]; free MMAE disrupts microtubules, leading to apoptosis. Such ADCs exploit the targeting specificity of monoclonal antibodies and the potency of MMAE to achieve cancer cell death while limiting systemic toxicity[4][6].

Other names
mAb104-MMAEmAb-104-MMAEmAb 104-MMAEmAb104 antibody–drug conjugatemAb104 vedotin (if the linker is vedotin)antibody-drug conjugate of mAb104 and MMAE
02

Targets

ERBB2 (Erb-b2 receptor tyrosine kinase 2)TUBB (Tubulin (alpha and beta subunits))

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