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SAT-122 is a small molecule inhibitor that disrupts the interaction between RAD51 and BRCA2, key proteins involved in homologous recombination DNA repair. By inhibiting RAD51, SAT-122 aims to sensitize cancer cells—particularly those resistant to PARP inhibitors—to DNA-damaging therapies. The drug is being developed by Satya Pharma Innovations for the treatment of solid tumors, with a focus on overcoming resistance mechanisms in cancers that have become refractory to existing treatments targeting DNA repair pathways[1][2][4].
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