Massive cancer sample collection aims to unlock new treatments
NCT ID NCT07543159
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study collects blood, tissue, and other samples from up to 900,000 people, including cancer patients, survivors, and those at high risk. The goal is to create a large biobank that researchers can use to better understand cancer and develop new tests and treatments. Participants provide samples over time, but no experimental treatment is given in this study.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 900,000 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Dec 2025
- Expected to finish
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Oct 2035
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Subjects diagnosed with or suspected of having cancerous disease, or from healthy, normal donors with the goal of aiding in biomarker research, early detection of disease, and development of new devices or therapies.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Subjects must be at least 18 years of age 2. Subjects must be deemed competent by a qualified clinical study researcher to provide legally documented informed consent 3. Subjects may or may not have active disease at the time of enrollment 4. Biospecimens collected under this protocol may be obtained from subjects with benign conditions, subjects who have been diagnosed with or suspected of having oncological diseases, infectious diseases, auto-immune diseases, endocrine disorders, as well as subjects from healthy normal donors. Exclusion Criteria: 4\) Subjects not meeting the inclusion criteria Additional inclusion and exclusion criteria may exist, specific to individual project plans, for each collection falling under this protocol. These criteria may include genetic mutation status, progression of disease, and prior lines of therapy among others.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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NYCBS
RECRUITINGShirley, New York, 11967, United States
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