Caris Biorepository Research Protocol

Sponsor
Caris Science, Inc. (Industry)
Overall Status
Recruiting
CT.gov ID
NCT01499394
Collaborator
(none)
100,000
7
180
14285.7
79.4

Study Details

Study Description

Brief Summary

The Biorepository for Caris Life Sciences is designed for the purpose of making quality biospecimens and associated clinical data available for research studies related to advancing precision medicine and improving care for patients.

The Caris Biorepository is a repository of prospectively collected biological specimens and associated clinical and demographic data gathered from multiple sources to be stored, used and shared for research. Caris Life Sciences will maintain the data and specimens and will control access to and use of the information and specimens by multiple individuals for multiple purposes which may evolve over time.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    The Caris Biorepository is an effort toward defining the future of medicine incorporating the discoveries of the genomic era by providing physicians, researchers and scientists access to quality human specimens and data aimed at improving human health and fighting disease. This will be accomplished through acquiring and sharing valuable biospecimen information and clinical outcomes in a collaborative, secure environment. The Caris Biorepository will bridge the gap and correlate human specimens with clinical and specimen data valuable to multiple and varying entities interested in advancing science with precision medicine by targeting disease treatments.

    The objective of this project is to develop and implement a state-of-the-science Biorepository that ensures molecular integrity and clinical relevance of human biospecimens used in research and clinical medicine. The Caris Biorepository will also provide vital biospecimens and data to internal researchers and external research collaborators such as government, academia and industry collaborators for the use of drug development discoveries, clinically relevant research trials, publications and posters, and the implementation of future healthcare policies. This project may also impact characterization of trends in practice patterns and their relation to patient outcomes as well as the economic implications of differing evaluation, treatment and management paradigms.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    100000 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    The Caris Biorepository Research Protocol
    Study Start Date :
    Nov 1, 2010
    Anticipated Primary Completion Date :
    Nov 1, 2020
    Anticipated Study Completion Date :
    Nov 1, 2025

    Arms and Interventions

    Arm Intervention/Treatment
    Normal

    Donor samples reflective of a "normal" non-disease state

    Disease state or condition

    Donor samples reflective of a known disease state or condition

    Outcome Measures

    Primary Outcome Measures

    1. Develop biorepository that ensures molecular integrity and clinical relevance of quality human biospecimens and associated clinical data. [5 years]

      Retention of biospecimen samples with DNA

    2. Implement release of specimens from biorepository for testing [5 years]

      Research for the purposes of cancer laboratory diagnostic tests.

    Secondary Outcome Measures

    1. Laboratory testing [5 years]

      DNA and RNA microarray

    2. Laboratory testing [5 years]

      Immunohistochemistry

    3. Laboratory testing [5 years]

      Gene and protein expression, proteomics and matabolomics

    4. Laboratory testing [5 years]

      Mutation analysis

    5. Laboratory testing [5 years]

      Experiemental lab testing for development of new diagnostic technology

    6. Laboratory testing [5 years]

      Microvesicle discovery, characterization and validation.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • 18 years of age or older

    • Capacity to provide informed consent

    Exclusion Criteria:
    • Due to the complexity of state and federal requirements governing the participation of prisoners in research, prisoners-patients will not be approached for participation in the Caris Biorepository.

    • Minor subjects will not be included in the Caris Biorepository, as it is possible biospecimens and data may be stored beyond the time limitations of assent and it may be impracticable to re-consent these subjects once they become adults.

    • Individuals who lack the capacity to give informed consent

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Phoebe Putney Memorial Hospital Albany Georgia United States 31701
    2 The Iowa Clinic, PC West Des Moines Iowa United States 50266
    3 Eastern Carolina Women's Center New Bern North Carolina United States 28562
    4 Advantage Clinical Research Nashville Tennessee United States 37203
    5 Overlake Hospital Bellevue Washington United States 98004
    6 Walla Walla Clinic Walla Walla Washington United States 99362
    7 CAMC Clinical Trials Charleston West Virginia United States 25304

    Sponsors and Collaborators

    • Caris Science, Inc.

    Investigators

    • Principal Investigator: Zoran Gatalica, MD, DSc, Caris Life Sciences

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Caris Science, Inc.
    ClinicalTrials.gov Identifier:
    NCT01499394
    Other Study ID Numbers:
    • TCBIO-001-0710
    First Posted:
    Dec 26, 2011
    Last Update Posted:
    Jan 23, 2020
    Last Verified:
    Jan 1, 2020

    Study Results

    No Results Posted as of Jan 23, 2020