UnknownNot applicableNCT04638751

ARGONAUT: Stool and Blood Sample Bank for Cancer Patients

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.

Checked against the public recordLast updated Apr 5, 2024 · Source: ClinicalTrials.gov

StatusUnknown
PhaseNot applicable
U.S. locations10
SponsorPersephone Biosciences
01
Study overview

What this study is about

Purpose
Not specified
Study type
Observational
Phase
Not applicable
Sponsor
Persephone Biosciences
Interventions being studied
Drug: Immunotherapy; Drug: Chemotherapy; Procedure: CRC surgical resection; Procedure: Colonoscopy
02
Explore related studies

How this study is categorized

These labels come from structured fields and exact terms in the public record.

03
Public criteria

Who may be able to participate

Inclusion Criteria: * 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 Criteria: * 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

Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.

04
Study sites

U.S. locations

  • Knowledge Research CenterOrange, California
  • SDG Clinical Research, IncSan Diego, California
  • Persephone Biosciences, Inc.San Diego, California
  • L&A Morales Healthcare, IncMiami, Florida
  • Baton Rouge General Medical CenterBaton Rouge, Louisiana
  • University Medical Center New OrleansNew Orleans, Louisiana
  • Mid-Hudson Medical ResearchNew Windsor, New York
  • Kroger Health, The Little ClinicCincinnati, Ohio
  • Southwest Family Medicine AssociatesDallas, Texas
  • Biopharma InformaticHouston, Texas

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Apr 5, 2024. Always confirm current availability with the study team.

View original record ↗