ESMO Congress 2024

September 13 – 17, 2024
Barcelona, Spain

BOOTH #608

Connect with Caris Life Sciences during ESMO Congress

Join Caris Life Sciences at the European Society for Medical Oncology (ESMO) in Barcelona, Spain. Visit us at booth #608 to uncover the latest breakthroughs in precision medicine. The findings demonstrate the power of Caris’ comprehensive multi-modal database to enable novel insights into cancer that could have profound effects on a patient’s diagnosis, prognosis, care plan and response to treatment.

  • Comprehensive molecular profiling – no matter the specimen type, tissue or blood:
    • Tissue: DNA, RNA and Protein biomarker analysis
    • Blood: Caris Assure™ featuring somatic tumor, clonal hematopoiesis and incidental germline* characterization
  • Whole exome and whole transcriptome sequencing for every patient
    • 23,000 genes via Whole Exome Sequencing (WES – DNA)
    • 61,000 transcripts via Whole Transcriptome Sequencing (WTS – RNA)
  • AI-Powered Predictive Signatures for metastatic CRC and tumor type confirmation
  • Accelerate therapeutic development with Caris Discovery™
    • Identify, develop and commercialize your next therapeutic targets
  • Make confident decisions with real-world, multi-modal data

Presentations and Posters

Caris and its collaborators from the biopharma industry and leading cancer centers, including those within the Precision Oncology Alliance™ (POA), will collectively present seven studies across a wide range of tumor types during ESMO.

Caris Abstracts and Presentation Schedule

Caris’ strong presence at ESMO 2024 demonstrates the clinical value of comprehensive molecular profiling and our commitment to transforming lives through research. Download the abstracts and presentation schedule, including a full list of summaries highlighting the research presented at ESMO 2024.

Schedule a Meeting with a Caris Expert

 Complete the form below to schedule a meeting and learn more about how Caris can support your precision medicine program.

Certain products and features may vary based on region or territory.

*Not a replacement for comprehensive germline testing. Incidental pathogenic alterations detected in ACMG recognized cancer genes are reported. Negative results do not imply the patient does not harbor a germline mutation.

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