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The clinical utility of the OMC Although clinical trials over years have established many front-line experience and clinical factors (genetics, pathology, physiology, etc.) for anticipating LADC patient responses to standard-of-care treatments, there is no simple and cost-effective assay for predicting therapy responses and identifying non-responders and short-term beneficiaries prior to the onset of therapies

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For example, drugs that restore the correct shape to mutant p53 have not progressed beyond Phase III clinical trials