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

Part of paid clinical trials in Boise, Idaho.

Sponsor
Sequenom, Inc.
Study ID
NCT02586389
Status
Recruiting

Conditions

  • Non-hematologic Cancer

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Study Details

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).

Key Dates

Start date
Oct 13, 2015
Status verified
Oct 2024
Primary completion
Oct 31, 2027
Completion
Oct 31, 2027

Study Design

Enrollment
3,000 participants (estimated)

Arms

  • Arm: Non-hematological Cancer Cohort
    Eligible subjects will have been previously diagnosed with a non-hematological cancer with tumor present at baseline blood draw.

Primary Outcome Measure

biospecimen sample collection for liquid biopsy assay development [ Time Frame: After cancer diagnosis through 5 years of standard of care follow-up visits ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Idaho UrologyBoiseIdaho--

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