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RC68-MC-VC-PAB-MMAE is a **novel antibody-drug conjugate (ADC)** composed of a humanized anti-EGFR monoclonal antibody (RC68) conjugated to monomethyl auristatin E (MMAE), a potent tubulin inhibitor, via a maleimidocaproyl-valine-citrulline-p-aminobenzyl (MC-VC-PAB) linker. The drug specifically targets **epidermal growth factor receptor (EGFR)** expressed on tumor cells. After binding to EGFR, the ADC is internalized and releases MMAE, which disrupts microtubule dynamics leading to cell death. It has demonstrated significant **anti-tumor activity** against EGFR-positive non-small cell lung cancer (NSCLC) and pancreatic cancer in preclinical models, showing greater efficacy than docetaxel and gemcitabine in respective xenograft models[1][5][7]. RC68-MC-VC-PAB-MMAE is distinct from other RC68 conjugates due to its MC-VC-PAB linker, which influences its pharmacodynamic and stability profile.
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