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

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a new treatment for people with cancer, immune checkpoint therapy, and other related conditions. The study is currently recruiting participants at 3 locations. People eligible for this study include aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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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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