ClinicalTrials.gg
Enrolling by invitationNCT07756320TARGETUpdated Aug 17, 2026

Precure Targeted Accrual and Rapid Growth in Enrollment Trial Study

An observational study in Exposure, Environmental and Genetic Predisposition, sponsored by Mayo Clinic. Enrolling by invitation at 1 site in United States. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-08-17.

Sponsored by Mayo Clinic · Observational

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Study type
Observational
Model
Ecologic or community
Time perspective
Prospective
Enrollment
100,000
Ages
18 Years and older
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-13

Among 86 studies in Genetic Predisposition to Disease with a site in United States — 36 open to participants now, 45 under way, none of them phase 3. Genetic Predisposition to Disease · United States.

Planned enrollment
2nd of 50
100,000 · median 560
Started
2026
with 8 others
Observational
50 of 86
23 open now
Primary completion
2030-12
later than 36 of 44 live
Registered
85th of 86
by date
Lead sponsor
4 of 86
Mayo Clinic

Among the 86 studies in Genetic Predisposition to Disease with a site in United States, this one is the 2nd largest by planned enrollment of the 50 observational ones that give a count, is one of 9 that started in 2026, is one of 50 observational ones, reaches primary completion later than 36 of the 44 other live ones, and was the 85th registered.

Genetic Predisposition to Disease

241 studies on the registry are indexed under Genetic Predisposition to Disease; 95 are open to participants now.

Browse Genetic Predisposition to Disease studies →

Open to participants now

36 of the 86 studies in Genetic Predisposition to Disease with a site in United States are open now. Recruiting first, the newest first:

31 more — sign in →

All 36 open studies →

A study can be open while its sites in United States have not opened yet or have stopped. Only those recruiting at a site in United States →

Who these studies take

Of the 71 Genetic Predisposition to Disease studies recruiting now, 36 (51%) set no upper age limit and 28 (39%) stop at 75 or younger; 25 take children under 18; 23 take healthy volunteers.

This study: 18 Years and older · all sexes · healthy volunteers too.

The full table on the hub →

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Watch this landscapeDownload CSVNarrow it in search →With an account: a weekly mail of what changed among 86 studies in Genetic Predisposition to Disease with a site in United States, or all of them as a file.
02

Study 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
03

Conditions studied

  • Exposure, Environmental
  • Genetic Predisposition
04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Mayo Clinic patients

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Age ≥ 18 years
  • Registered Mayo Clinic patient
  • Able to provide

Exclusion criteria

Exclusion Criteria:

  • Other co-morbidity that, in physician's opinion, would interfere with patient's ability to participate in the study
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Observational model
Ecologic or community
Time perspective
Prospective
Enrollment
100,000 participants (estimated)
Patient registry
No
Biospecimen retention
Samples with dna
06

What researchers measure

Primary outcomes

  1. Number of participants (up to 100,000) who provide biospecimens and have associated environmental exposure and phenotypic data successfully linked and stored within the biorepository and research database for future research.

    Time frame: Up to 5 years

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Aug 2026 (actual). Primary completion is estimated for Dec 2030, 52 months after the start.

Of 80 non-industry observational studies under Genetic Predisposition to Disease, half reached primary completion within 96 months of starting (the median), counting those still running; a quarter within 52. This study's planned 52 months is below that.

Counting every sponsor, half of 82 studies reached it within 96 months; a quarter within 52.

How these figures are worked out, and which studies are left out of them.

Registered
Jul 28, 2026
First posted
Aug 10, 2026
StartActual
Aug 7, 2026
Primary completionEst.
Dec 2030
CompletionEst.
Dec 2035
Last update
Aug 17, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 17, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07756320
Lead sponsor
Mayo Clinic
Responsible party
Konstantinos N. Lazaridis, M.D. (Executive Director, Center for Individualized Medicine, Mayo Clinic) — Principal investigator
First posted
Aug 10, 2026
Start date
Aug 7, 2026
Primary completion
Dec 2030 (estimated)
Completion
Dec 2035 (estimated)
Last update
Aug 17, 2026

Study contacts

Konstantinos N. Lazaridis, M.D.
principal investigator · Mayo Clinic

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Interested in this study?

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No contact was published for this record. The registry link below has the sponsor’s details.

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Discussion

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