RecruitingNCT06635954

A Prospective Real World Evidence Study (PROWES) for Concordance Rate of Blood-based 3D Genome Conformation Mapping (Episwitch CiRT®) to Identify Likelihood of Response and Actual Response Rates to PD-(L)-1 Checkpoint Inhibitors Across Multiple Oncological Indications.


Sponsor

Oxford Biodynamics Inc.

Enrollment

2,000 participants

Start Date

May 14, 2024

Study Type

OBSERVATIONAL

Conditions

Summary

The purpose of this research is to test whether a blood-based 3D genome conformation mapping test called the Episwitch CiRT® can help to identify likelihood of response to PD-(L)-1 checkpoint inhibitors (a class of cancer drugs) across multiple oncological indications by comparing the results to actual treatment responses for cancer patients.


Eligibility

Min Age: 18 Years

Inclusion Criteria7

  • 18 years of age or older
  • Stage III or IV cancer
  • Selected by their healthcare provider to receive the Episwitch CiRT® test according to the current evidence-based schedule (per protocol) as part of their standard of practice.
  • ECOG performance status ≤ 2
  • Clinically eligible for ICI therapy
  • Able to read, understand and provide written informed consent.
  • Willing and able to comply with the study requirements

Exclusion Criteria3

  • Pregnant or breastfeeding
  • History of bone marrow or organ transplant
  • Contra indication for receiving Immune Check Point inhibitor.

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Locations(3)

Eastern Connecticut Hematology and Oncology

Norwich, Connecticut, United States

Cancer Center of Middle Georgia

Dublin, Georgia, United States

Carolina Blood and Cancer Care Associates

Rock Hill, South Carolina, United States

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NCT06635954


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