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Sample Collection for Ongoing Research and Product Evaluation Study
NCT07318051 · Natera, Inc.
In plain English
Click the button to translate this study into plain language — what it is, who qualifies, and what participation looks like.
Official title
Sample Collection for Ongoing Research and Product Evaluation (SCORE) Study
About this study
The study is designed to evaluate the clinical performance of Natera's molecular residual disease (MRD) assays in detecting ctDNA across multiple solid tumor types. The goal is to assess the ability of the assay to identify minimal residual disease, monitor disease recurrence, and evaluate treatment response following standard-of-care therapy. No individual test results from the study testing will be provided to participants or their treating clinicians.
Participants who meet eligibility criteria for the SCORE study will be invited to enroll and must provide written informed consent prior to undergoing any study procedures. Participants will provide study-specific blood samples.
The SCORE study includes three participant cohorts:
* Cohort A - Surgical with Curative Intent
* Cohort B - Neoadjuvant Therapy
* Cohort C - Metastatic/No Surgery
Participants may be followed for up to eight years. During the first three years, blood samples will be collected periodically, approximately every six weeks, for up to two years after surgery or completion of primary treatment. Participants will have data-only follow-up visits at one and five years after the final blood collection.
Tissue Sample Collection Residual tissue samples, collected as part of standard-of-care procedures, will also be obtained for study purposes.
Eligibility criteria
Inclusion Criteria:
1. 18 years of age or older.
2. Any patient that has an untreated primary solid malignancy within the following cohorts:
1. Breast cancer
2. Lung cancer
3. Muscle invasive bladder cancer
4. Rectal cancer
5. Pancreatic cancer
6. Ovarian cancer
7. Gastroesophageal cancer
8. Prostate cancer
9. Melanoma
10. Hepatic/liver cancer
11. Uterine/endometrial cancer
12. Head and neck Cancer
3. The participant has a suspected primary malignancy of pancreatic, endometrial, bladder, or ovarian cancer based on imaging.
4. Eastern Cooperative Oncology Group performance status ≤ 2.
5. Able to tolerate venipuncture for research blood draw(s).
6. Consent to provide residual tumor tissue for research.
7. Willing and able to comply with the study requirements.
8. Signed informed consent(s) must be obtained prior to participation in the study.
Exclusion Criteria:
1. Pregnant or breastfeeding.
2. Prior history and treatment for any cancer within the past year or has another active cancer, with the exception of participants who have undergone surgical removal of skin squamous cell or basal cell cancers.
3. Has initiated postoperative systemic treatment.
4. At time of enrollment, has undergone or plans to undergo any ctDNA testing to assess molecular residual disease, with the exception of comprehensive genomic profiling for therapeutic selection.
5. History of bone marrow or organ transplant.
6. Serious medical conditions that may adversely affect ability to participate in the study.
Study design
Enrollment target: 9600 participants
Age groups: adult, older_adult
Timeline
Starts: 2025-07-21
Estimated completion: 2035-01
Last updated: 2026-01-15
Primary outcomes
- • Primary Outcome - Collection of Blood and Residual Tissue Specimens for Cancer Assay Development (8 years)
Sponsor
Natera, Inc. · industry
Contacts & investigators
ContactSCORE Study team · contact · contactscorestudy@natera.com · 650-489-9050
All locations (1)
Natera, Inc.Recruiting
Austin, Texas, United States