Tempus AI Announces Publication Of HLA-LOH Investigational Assay Validation Study In npj Precision Oncology; Study Demonstrates Detection Of HLA Loss Of Heterozygosity Using Tempus' FDA-Approved xT CDx Assay For Prognostic And Therapeutic Opportunities In Solid Tumor Patients
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Tempus AI has announced the publication of a validation study for its HLA-LOH investigational assay in npj Precision Oncology. The study demonstrates the detection of HLA loss of heterozygosity using Tempus' FDA-approved xT CDx assay, which offers prognostic and therapeutic opportunities for solid tumor patients.
August 08, 2024 | 12:35 pm
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Tempus AI's publication of a validation study for its HLA-LOH investigational assay in npj Precision Oncology highlights the capabilities of its FDA-approved xT CDx assay. This development could enhance the company's reputation in precision oncology and potentially increase demand for its assay.
The publication of the validation study in a reputable journal like npj Precision Oncology underscores the scientific credibility and potential clinical utility of Tempus AI's xT CDx assay. This could lead to increased adoption by oncologists and healthcare providers, thereby boosting the company's revenues and market position.
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