A Registry to Collect Human Bio-Specimens from Healthy Volunteers to Support Clinical Protocol Development

Overview

  • Study type

    Observational
  • Study IDs

  • Describes the nature of a clinical study. Types include:

    • Observational study — observes people and measures outcomes without affecting results.
    • Interventional study (clinical trial) — studies new tests, treatments, drugs, surgical procedures or devices.
    • Medical records research — uses historical information collected from medical records of large groups of people to study how diseases progress and which treatments and surgeries work best.
  • Site IRB
    • Jacksonville, Florida: 16-000881
    Sponsor Protocol Number: 16-000881

About this study

The purpose of this registry is to collect human biospecimens for the support of new clinical protocol development and produce clinical grade cells and tissue for future clinical trials.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. If you need assistance understanding the eligibility criteria, please contact the study team.

See eligibility criteria

Inclusion Criteria

  • Adults between 18 and 70 years
  • Free from risk factors for and clinical evidence of relevant communicable diseases
  • Free from communicable disease risks associated with xenotransplantation
  • Tests negative or non-reactive for relevant communicable disease agents

Participating Mayo Clinic locations

Study statuses change often. Please contact us for help.

Mayo Clinic Location Status Contact

Jacksonville, Fla.

Mayo Clinic principal investigator

Abba Zubair, M.D., Ph.D.

Open for enrollment

Contact information:

Rebecca Lefavor

(904)953-1867

Lefavor.Rebecca@mayo.edu

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CLS-20359597

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