Caris Biorepository Research Protocol
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.
Conditions:
🦠 Cancer
🗓️ Study Start (Actual) November 2010
🗓️ Primary Completion (Estimated) November 2020
✅ Study Completion (Estimated) November 2025
👥 Enrollment (Estimated) 100000
🔬 Study Type OBSERVATIONAL
📊 Phase N/A
Locations:
📍 Albany, Georgia, United States
📍 West Des Moines, Iowa, United States
📍 New Bern, North Carolina, United States
📍 Nashville, Tennessee, United States
📍 Bellevue, Washington, United States
📍 Walla Walla, Washington, United States
📍 Charleston, West Virginia, United States

📋 Eligibility Criteria

Description

    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
Ages Eligible for Study: 18 Years to N/A (ADULT, OLDER_ADULT)
Sexes Eligible for Study: ALL
Accepts Healthy Volunteers: Yes

🗓️ Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

  • First Submitted 16 December 2011
  • First Submitted that Met QC Criteria 22 December 2011
  • First Posted 26 December 2011

Study Record Updates

  • Last Update Submitted that Met QC Criteria 21 January 2020
  • Last Update Posted 23 January 2020
  • Last Verified January 2020