Actively Recruiting

Age: 18Years +
All Genders
NCT02586389

Specimen Collection from Patients with Non-Hematologic Cancer for Use in Development of a Liquid Biopsy Assay

Led by Sequenom, Inc. · Updated on 2024-10-16

3000

Participants Needed

1

Research Sites

628 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This specimen collection is designed to obtain whole blood and tumor tissue from subjects diagnosed with cancer for the purpose of the development of a noninvasive liquid biopsy assay using next generation sequencing (NGS).

CONDITIONS

Official Title

Specimen Collection from Patients with Non-Hematologic Cancer for Use in Development of a Liquid Biopsy Assay

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Subject is 18 years of age or older
  • Subject is willing to provide written informed consent
  • Subject has a diagnosis of a non-hematologic cancer with tumor present in the body
  • Subject has either residual tumor tissue available for testing; or genomic profiling results from an approved tumor biopsy test; or a biopsy or surgery scheduled after the baseline visit to provide tumor tissue
  • Subject is able to provide whole blood samples at baseline and follow-up visits as judged by the investigator
Not Eligible

You will not qualify if you...

  • Underwent curative-intent surgery for the current tumor before the baseline visit
  • Received chemotherapy, hormone receptor blocking therapy, or radiation therapy before the baseline visit
  • Had an invasive procedure like biopsy, surgery, or thermal ablation within 7 days before any blood collection visit
  • Has any medical or mental condition interfering with the ability to give informed consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Idaho Urology

Boise, Idaho, United States

Actively Recruiting

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Research Team

G

Graham McLennan

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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