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R7072 is a fully human, glycoengineered monoclonal antibody (mAb) developed by Roche that targets the insulin-like growth factor 1 receptor (IGF-1R). It is an afucosylated (glycoengineered) version of the parental antibody R1507, designed to exhibit enhanced antibody-dependent cell-mediated cytotoxicity (ADCC) activity. R7072 binds to IGF-1R and blocks the binding of its ligands, IGF-1 and IGF-2, thereby inhibiting downstream PI3K-AKT and RAS-RAF-MAPK signaling pathways that drive tumor cell proliferation and survival. Preclinical studies have evaluated R7072 as a monotherapy and in combination with anti-HER2 therapies (such as trastuzumab or trastuzumab emtansine) to overcome resistance in HER2-positive breast cancer models, as well as in bispecific formats (such as XGFR) targeting both EGFR and IGF-1R.
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