Ignite Creation Date:
2026-03-26 @ 3:18 PM
Ignite Modification Date:
2026-03-30 @ 3:17 AM
Study NCT ID:
NCT07318051
Status:
RECRUITING
Last Update Posted:
2026-01-15
First Post:
2025-12-19
Is NOT Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
Sample Collection for Ongoing Research and Product Evaluation Study
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2026-03-25'}, 'conditionBrowseModule': {'meshes': [{'id': 'D001943', 'term': 'Breast Neoplasms'}, {'id': 'D008175', 'term': 'Lung Neoplasms'}, {'id': 'D012004', 'term': 'Rectal Neoplasms'}, {'id': 'D010190', 'term': 'Pancreatic Neoplasms'}, {'id': 'D010051', 'term': 'Ovarian Neoplasms'}, {'id': 'D011471', 'term': 'Prostatic Neoplasms'}, {'id': 'D008545', 'term': 'Melanoma'}, {'id': 'D006258', 'term': 'Head and Neck Neoplasms'}, {'id': 'D014594', 'term': 'Uterine Neoplasms'}, {'id': 'D008113', 'term': 'Liver Neoplasms'}], 'ancestors': [{'id': 'D009371', 'term': 'Neoplasms by Site'}, {'id': 'D009369', 'term': 'Neoplasms'}, {'id': 'D001941', 'term': 'Breast Diseases'}, {'id': 'D012871', 'term': 'Skin Diseases'}, {'id': 'D017437', 'term': 'Skin and Connective Tissue Diseases'}, {'id': 'D012142', 'term': 'Respiratory Tract Neoplasms'}, {'id': 'D013899', 'term': 'Thoracic Neoplasms'}, {'id': 'D008171', 'term': 'Lung Diseases'}, {'id': 'D012140', 'term': 'Respiratory Tract Diseases'}, {'id': 'D015179', 'term': 'Colorectal Neoplasms'}, {'id': 'D007414', 'term': 'Intestinal Neoplasms'}, {'id': 'D005770', 'term': 'Gastrointestinal Neoplasms'}, {'id': 'D004067', 'term': 'Digestive System Neoplasms'}, {'id': 'D004066', 'term': 'Digestive System Diseases'}, {'id': 'D005767', 'term': 'Gastrointestinal Diseases'}, {'id': 'D007410', 'term': 'Intestinal Diseases'}, {'id': 'D012002', 'term': 'Rectal Diseases'}, {'id': 'D004701', 'term': 'Endocrine Gland Neoplasms'}, {'id': 'D010182', 'term': 'Pancreatic Diseases'}, {'id': 'D004700', 'term': 'Endocrine System Diseases'}, {'id': 'D010049', 'term': 'Ovarian Diseases'}, {'id': 'D000291', 'term': 'Adnexal Diseases'}, {'id': 'D005831', 'term': 'Genital Diseases, Female'}, {'id': 'D052776', 'term': 'Female Urogenital Diseases'}, {'id': 'D005261', 'term': 'Female Urogenital Diseases and Pregnancy Complications'}, {'id': 'D000091642', 'term': 'Urogenital Diseases'}, {'id': 'D005833', 'term': 'Genital Neoplasms, Female'}, {'id': 'D014565', 'term': 'Urogenital Neoplasms'}, {'id': 'D000091662', 'term': 'Genital Diseases'}, {'id': 'D006058', 'term': 'Gonadal Disorders'}, {'id': 'D005834', 'term': 'Genital Neoplasms, Male'}, {'id': 'D005832', 'term': 'Genital Diseases, Male'}, {'id': 'D011469', 'term': 'Prostatic Diseases'}, {'id': 'D052801', 'term': 'Male Urogenital Diseases'}, {'id': 'D018358', 'term': 'Neuroendocrine Tumors'}, {'id': 'D017599', 'term': 'Neuroectodermal Tumors'}, {'id': 'D009373', 'term': 'Neoplasms, Germ Cell and Embryonal'}, {'id': 'D009370', 'term': 'Neoplasms by Histologic Type'}, {'id': 'D009380', 'term': 'Neoplasms, Nerve Tissue'}, {'id': 'D018326', 'term': 'Nevi and Melanomas'}, {'id': 'D012878', 'term': 'Skin Neoplasms'}, {'id': 'D014591', 'term': 'Uterine Diseases'}, {'id': 'D008107', 'term': 'Liver Diseases'}]}}, 'protocolSection': {'designModule': {'bioSpec': {'retention': 'SAMPLES_WITH_DNA', 'description': 'Whole blood and tissue samples'}, 'studyType': 'OBSERVATIONAL', 'designInfo': {'timePerspective': 'PROSPECTIVE', 'observationalModel': 'COHORT'}, 'enrollmentInfo': {'type': 'ESTIMATED', 'count': 9600}, 'patientRegistry': False}, 'statusModule': {'overallStatus': 'RECRUITING', 'startDateStruct': {'date': '2025-07-21', 'type': 'ACTUAL'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2025-12', 'completionDateStruct': {'date': '2035-01', 'type': 'ESTIMATED'}, 'lastUpdateSubmitDate': '2026-01-13', 'studyFirstSubmitDate': '2025-12-19', 'studyFirstSubmitQcDate': '2025-12-19', 'lastUpdatePostDateStruct': {'date': '2026-01-15', 'type': 'ACTUAL'}, 'studyFirstPostDateStruct': {'date': '2026-01-05', 'type': 'ACTUAL'}, 'primaryCompletionDateStruct': {'date': '2035-01', 'type': 'ESTIMATED'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Primary Outcome - Collection of Blood and Residual Tissue Specimens for Cancer Assay Development', 'timeFrame': '8 years', 'description': 'To collect de-identified whole blood and residual tissue specimens for research use and the development of blood-based cancer monitoring and detection assays.'}], 'secondaryOutcomes': [{'measure': 'Secondary Outcome - Collection of Blood and Residual Tissue Specimens for Disease Assay Development', 'timeFrame': '8 years', 'description': 'To collect de-identified whole blood and residual tissue specimens for research use and the development of blood-based disease assays.'}]}, 'oversightModule': {'isFdaRegulatedDrug': False, 'isFdaRegulatedDevice': False}, 'conditionsModule': {'keywords': ['Breast cancer', 'Lung cancer', 'Muscle invasive bladder cancer', 'Rectal cancer', 'Pancreatic cancer', 'Ovarian cancer', 'Gastroesophageal cancer', 'Prostate cancer', 'Melanoma', 'Head and Neck cancer', 'Uterine cancer', 'Liver cancer'], 'conditions': ['Breast Cancer', 'Lung Cancer', 'Muscle Invasive Bladder Cancer', 'Rectal Cancer', 'Pancreatic Cancer', 'Ovarian Cancer', 'Gastroesophageal Cancer', 'Prostate Cancer', 'Melanoma', 'Head and Neck Cancer', 'Uterine Cancer', 'Liver Cancer']}, 'descriptionModule': {'briefSummary': "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.", 'detailedDescription': "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.\n\nParticipants 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.\n\nThe SCORE study includes three participant cohorts:\n\n* Cohort A - Surgical with Curative Intent\n* Cohort B - Neoadjuvant Therapy\n* Cohort C - Metastatic/No Surgery\n\nParticipants 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.\n\nTissue Sample Collection Residual tissue samples, collected as part of standard-of-care procedures, will also be obtained for study purposes."}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'minimumAge': '18 Years', 'samplingMethod': 'NON_PROBABILITY_SAMPLE', 'studyPopulation': 'Participants 18 years of age or older diagnosed with malignant, invasive solid tumors prior to receiving treatment.', 'healthyVolunteers': False, 'eligibilityCriteria': 'Inclusion Criteria:\n\n1. 18 years of age or older.\n2. Any patient that has an untreated primary solid malignancy within the following cohorts:\n\n 1. Breast cancer\n 2. Lung cancer\n 3. Muscle invasive bladder cancer\n 4. Rectal cancer\n 5. Pancreatic cancer\n 6. Ovarian cancer\n 7. Gastroesophageal cancer\n 8. Prostate cancer\n 9. Melanoma\n 10. Hepatic/liver cancer\n 11. Uterine/endometrial cancer\n 12. Head and neck Cancer\n3. The participant has a suspected primary malignancy of pancreatic, endometrial, bladder, or ovarian cancer based on imaging.\n4. Eastern Cooperative Oncology Group performance status ≤ 2.\n5. Able to tolerate venipuncture for research blood draw(s).\n6. Consent to provide residual tumor tissue for research.\n7. Willing and able to comply with the study requirements.\n8. Signed informed consent(s) must be obtained prior to participation in the study.\n\nExclusion Criteria:\n\n1. Pregnant or breastfeeding.\n2. 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.\n3. Has initiated postoperative systemic treatment.\n4. 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.\n5. History of bone marrow or organ transplant.\n6. Serious medical conditions that may adversely affect ability to participate in the study.'}, 'identificationModule': {'nctId': 'NCT07318051', 'acronym': 'SCORE', 'briefTitle': 'Sample Collection for Ongoing Research and Product Evaluation Study', 'organization': {'class': 'INDUSTRY', 'fullName': 'Natera, Inc.'}, 'officialTitle': 'Sample Collection for Ongoing Research and Product Evaluation (SCORE) Study', 'orgStudyIdInfo': {'id': '25-081-NCP'}}, 'contactsLocationsModule': {'locations': [{'zip': '78753', 'city': 'Austin', 'state': 'Texas', 'status': 'RECRUITING', 'country': 'United States', 'contacts': [{'name': 'Jamie McKenzie, MD', 'role': 'CONTACT', 'email': 'contactscorestudy@natera.com', 'phone': '650-489-9050'}], 'facility': 'Natera, Inc.', 'geoPoint': {'lat': 30.26715, 'lon': -97.74306}}], 'centralContacts': [{'name': 'SCORE Study team', 'role': 'CONTACT', 'email': 'contactscorestudy@natera.com', 'phone': '650-489-9050'}]}, 'ipdSharingStatementModule': {'ipdSharing': 'NO'}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'Natera, Inc.', 'class': 'INDUSTRY'}, 'responsibleParty': {'type': 'SPONSOR'}}}}