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Clinical Trials/NCT07332598
NCT07332598Enrolling By InvitationNot Applicable

Mayo Clinic Precure - Prospective Study

Mayo Clinic1 site in 1 country100,000 target enrollmentStarted: January 19, 2026Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Enrolling By Invitation
Enrollment
100,000
Locations
1
Primary Endpoint
Build a comprehensive, multi-omics and phenotype dataset

Study Overview

Brief Summary

The goal of this observational study is to 1) better understand and predict biological processes before disease begins or is identified, 2) study genomic and environmental contributors to disease, 3) identify ways to stop disease advancement before it becomes serious or complex, and 4) identify potential targets for disease therapy.

Participants will be asked to:

  • collect biological samples,
  • download a mobile app,
  • collect speech (voice) recordings, and
  • complete surveys

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Other

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Age ≥ 18 years
  • Registered Mayo Clinic patient
  • Able to provide informed written consent
  • Able to receive mail and packages within a United States (US) state
  • Able to collect and ship samples within a US state via FedEx for overnight delivery

Exclusion Criteria

  • Active hematological cancer or history of a hematological cancer
  • Allogeneic Bone Marrow Transplant (autologous bone marrow transplant recipients are acceptable if collected at least one month after transplant)
  • Other co-morbidity that, in physician's opinion, would interfere with patient's ability to participate in the study (e.g., reduced ability to comprehend, i.e., dementia, intellectual disability, etc.)

Arms & Interventions

Suspected Genetic Predisposition or Multi-Omics Contribution

Patients with a diagnosis or phenotype with the potential for association with a genetic predisposition or Multi-Omics Contribution

Health Control

Patients with no diagnosis associated with a genetic predisposition or Multi-Omics Contribution.

Outcomes

Primary Outcomes

Build a comprehensive, multi-omics and phenotype dataset

Time Frame: Up to 5 years

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Konstantinos N. Lazaridis, M.D.

Executive Director, Center for Individualized Medicine

Mayo Clinic

Study Sites (1)

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