Vincere Biobank Research Protocol
1 other identifier
observational
5,000
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jul 2023
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 12, 2023
CompletedStudy Start
First participant enrolled
July 18, 2023
CompletedFirst Posted
Study publicly available on registry
July 20, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2033
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 31, 2038
December 7, 2023
December 1, 2023
10.5 years
July 12, 2023
December 6, 2023
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Biobank
Collect quality biospecimens with associated clinical data for research studies related to improving medicine and care to the patient, including cancer screening, treatment, and care.
10 years
Study Arms (2)
Normal
Participants and donor samples without disease (ex: non-cancer)
Disease state or condition
Participants and donor samples with known disease or condition (ex: cancer)
Eligibility Criteria
Adults age 18 years and older of any gender and demographic group, including both healthy participants and those with disease.
You may qualify if:
- 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
You may not qualify if:
- Minors, under the age of 18 years
- Individuals who lack the capacity to give informed consent
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Vincere Cancer Center
Scottsdale, Arizona, 85260, United States
Biospecimen
Current blood (plasma, red blood cells), urine, and/or tissue; with the opportunity to collect other biospecimens
MeSH Terms
Conditions
Study Officials
- PRINCIPAL INVESTIGATOR
Vershalee Shukla, MD
Vincere Cancer Center
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 12, 2023
First Posted
July 20, 2023
Study Start
July 18, 2023
Primary Completion (Estimated)
December 31, 2033
Study Completion (Estimated)
December 31, 2038
Last Updated
December 7, 2023
Record last verified: 2023-12