Recruiting NCT05954299
Vincere Biobank Research Protocol
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Cancer. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Overview
The Vincere Biobank aims to make quality biospecimens and associated clinical data available for research studies related to advancing medicine and improving care for patients, including cancer screening, treatment, and care.
Primary outcome measures
- Biobank [Time frame: 10 years]
Eligibility criteria
Inclusion criteria
- 18 years of age or older; any gender
- Able to donate a blood, urine, tissue, and/or other biospecimen sample
- Able to provide informed consent to participate in the study
Exclusion criteria
- Minors, under the age of 18 years
- Individuals who lack the capacity to give informed consent
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Observational model
- Cohort
Study locations
United States · 1 center
- Vincere Cancer Center — Scottsdale
Identifiers
NCT: NCT05954299 · VCC-BIOBANK-001