xT CDx genomic profiling

by Tempus AIUS

Give every solid-tumour patient a full genetic readout that points to the right drug or trial, and turn millions of such tests into data that speeds up new cancer drugs.

ScalingStage 5 of 5

FDA-approved for tumour-only and tumour-normal use (May 2026); oncology test volume +31% in Q2 2026.

Updated 20 Jul 2026Checked 11 Oct0 updates this week

Milestones

Next · Personalis acquisition closes
  1. Tempus founded in Chicago2015Complete.
  2. FDA approves xT CDx (tumour plus matched normal)1 May 2023Complete.
  3. Nasdaq listing (TEM)14 Jun 2024Complete.
  4. Ambry Genetics acquisition completedFeb 2025Complete.
  5. FDA approves tumour-only use of xT CDx29 May 2026Complete.
  6. Personalis acquisition closesTarget Q4 2026Current milestone.
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