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Tempus uses multiple important sources of data relevant to drug development. Our current platform includes molecular, clinical, and pathology slide imaging data from real-world care of today. Current examples of molecular data include: Tumor/normal DNA sequencing (600+ genes)
The Tempus algorithmic test platform leverages our molecular and clinical database, CAP/CLIA lab, and clinician network to develop tests that help inform the treatment of cancer patients.
Tempus Labs Inc (Tempus) is a healthcare technology company, which collects and analyzes molecular, clinical and genomic data through the utilization of artificial intelligence technology.
Tempus utilizes a standardized clinical trial agreement, rate card, feasibility process, informed consent form (ICF), and a central IRB along with a team of dedicated research liaisons to streamline activities for study start-up. Site activated in 10 days on average.
Costs vary, but are commonly $300 or higher. You can request to be evaluated for a Tempus test from the comfort of your own home. If approved, the test is ordered by a licensed provider.

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The Tempus nP test is done through a saliva test. Once your provider orders a test for you, you will provide a saliva sample and send it back to our lab.
Once Tempus receives your sample, your provider will receive a report of your results in about 2 weeks. This report will provide your healthcare provider with information about your genes and how they may influence your bodys metabolism of certain medications.
Tempus reports on relevant therapeutic indications for detected somatic or gene expression alterations for which there is clinical evidence linking a given alteration to any FDA-approved therapy in the cancer under study, or another cancer, and for alterations associated with a known or suspected resistance to a

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