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MOS105 is a small molecule MDM2 inhibitor developed by Mosaic Therapeutics for the treatment of p53 wild-type (WT) hematological malignancies, including Acute Myeloid Leukemia (AML) and Myelodysplastic Syndromes (MDS). The drug functions by disrupting the interaction between the E3 ubiquitin ligase MDM2 and the tumor suppressor protein p53. In p53 WT cancers, MDM2 is often overexpressed, leading to the constitutive degradation of p53; MOS105 stabilizes p53, allowing it to activate downstream pathways involved in cell cycle arrest and apoptosis. Currently in IND-enabling studies, MOS105 is being positioned for use in combination therapy regimens.
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