RecruitingNCT04638751

ARGONAUT: Stool and Blood Sample Bank for Cancer Patients

ARGONAUT: Development and Analysis of a Blood and Stool Sample Bank for Cancer Patients, Enabling the Systematic Study of the Effect of Gut Microbiomes on Response to Treatment


Sponsor

Persephone Biosciences

Enrollment

5,000 participants

Start Date

Jul 1, 2022

Study Type

OBSERVATIONAL

Conditions

Summary

ARGONAUT is a longitudinal, prospective, observational study that will enroll up to 5,000 advanced-stage cancer patients of diverse racial backgrounds to collect data used to develop precision microbiome medicines and for the identification of clinically actionable cancer-specific biomarkers to guide therapeutic decisions. Four types of solid tumor cancers will be profiled including non-small cell lung cancer (NSCLC), triple negative breast cancer (TNBC), colorectal cancer (CRC) and pancreatic cancer. Healthy control subjects without a cancer diagnosis will also be studied, comprised of individuals at high risk for CRC and healthy individuals at low risk for CRC. Risk assessment will be based on family history or past neoplastic findings during CRC screening. Data collected from this study will be used to develop the most effective new therapies, via microbiome optimization, all to the benefit of patients and the physicians treating them. Stool and blood samples will be collected longitudinally and analyzed to determine the impact of gut microbiome composition and function on the immune system and efficacy of the treatment. Currently enrolling the CRC, high risk, and low risk cohorts. Subjects who meet the entry criteria will provide up to 5 samples each of blood and stool over a 2-year period. Approximately 10%-20% of the subjects will provide colon tissue samples, either from research biopsies during Standard of Care (SOC) screening colonoscopy or retained surgical tissue from colectomy. Electronic health records will be obtained at various times for up to 8 years, to collect tumor imaging results and any other updated medical data, with no additional samples collected. In select cases, stool and blood samples will be collected beyond 2 years.


Eligibility

Min Age: 18 Years

Inclusion Criteria2

  • Men or women who are ≥ 18 years old with stage III or stage IV non-small cell lung cancer (NSCLC), colorectal cancer, triple-negative breast cancer, or pancreatic cancer treated by a particular cancer treatment for the first time, OR healthy subjects undergoing a standard of care colonoscopy
  • Subjects able to provide written informed consent

Exclusion Criteria4

  • Subjects with known HIV, Hepatitis A, Hepatitis B, Hepatitis C, or SARS-CoV2
  • Subjects without the mental capacity to complete either a written or online questionnaire, alone or with assistance, or make sound decisions
  • Women who are pregnant or who plan on becoming pregnant
  • Women who are nursing

Interventions

DRUGImmunotherapy

Checkpoint inhibitor

DRUGChemotherapy

Any form of chemotherapy

PROCEDURECRC surgical resection

Surgical resection to remove colorectal cancer

PROCEDUREColonoscopy

Standard-of-care colonoscopy for CRC screening


Locations(10)

Knowledge Research Center

Orange, California, United States

SDG Clinical Research, Inc

San Diego, California, United States

Persephone Biosciences, Inc.

San Diego, California, United States

L&A Morales Healthcare, Inc

Miami, Florida, United States

Baton Rouge General Medical Center

Baton Rouge, Louisiana, United States

University Medical Center New Orleans

New Orleans, Louisiana, United States

Mid-Hudson Medical Research

New Windsor, New York, United States

Kroger Health, The Little Clinic

Cincinnati, Ohio, United States

Southwest Family Medicine Associates

Dallas, Texas, United States

Biopharma Informatic

Houston, Texas, United States

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NCT04638751


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