Actively Recruiting

Age: 18Years +
All Genders
NCT07318051

Sample Collection for Ongoing Research and Product Evaluation Study

Led by Natera, Inc. · Updated on 2026-01-15

9600

Participants Needed

1

Research Sites

493 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The SCORE study is a prospective, multi-site clinical trial designed to collect blood and tissue samples, along with relevant clinical data, from participants diagnosed with various solid tumors. The collected specimens and information will be used to evaluate the clinical performance of Natera's molecular residual disease (MRD) testing across multiple cancer types. The study aims to assess the ability of Natera's assays to detect circulating tumor DNA (ctDNA) as a marker for disease recurrence and treatment response.

CONDITIONS

Official Title

Sample Collection for Ongoing Research and Product Evaluation Study

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • 18 years of age or older
  • Diagnosed with untreated primary solid malignancy in breast, lung, muscle invasive bladder, rectal, pancreatic, ovarian, gastroesophageal, prostate, melanoma, hepatic/liver, uterine/endometrial, or head and neck cancer
  • Suspected primary malignancy of pancreatic, endometrial, bladder, or ovarian cancer based on imaging
  • Eastern Cooperative Oncology Group performance status 2 or less
  • Able to tolerate venipuncture for research blood draws
  • Consent to provide residual tumor tissue for research
  • Willing and able to comply with study requirements
  • Signed informed consent obtained prior to participation
Not Eligible

You will not qualify if you...

  • Pregnant or breastfeeding
  • Prior history and treatment for any cancer within the past year or having another active cancer, except surgical removal of skin squamous cell or basal cell cancers
  • Initiated postoperative systemic treatment
  • Undergoing or planning to undergo ctDNA testing to assess molecular residual disease, except comprehensive genomic profiling for therapy selection
  • History of bone marrow or organ transplant
  • Serious medical conditions that may affect ability to participate

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

Natera, Inc.

Austin, Texas, United States, 78753

Actively Recruiting

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Research Team

S

SCORE Study team

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

0

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