- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05954299
Vincere Biobank Research Protocol
December 6, 2023 updated by: Vincere Cancer Center
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.
Study Overview
Status
Recruiting
Conditions
Study Type
Observational
Enrollment (Estimated)
5000
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Christine Lau, MD
- Phone Number: 480-306-5390
- Email: drlau@vincerecancer.com
Study Locations
-
-
Arizona
-
Scottsdale, Arizona, United States, 85260
- Recruiting
- Vincere Cancer Center
-
Principal Investigator:
- Vershalee Shukla, MD
-
Contact:
- Christine Lau, MD
- Phone Number: 480-306-5390
- Email: drlau@vincerecancer.com
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
Adults age 18 years and older of any gender and demographic group, including both healthy participants and those with disease.
Description
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
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
|
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)
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Biobank
Time Frame: 10 years
|
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
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Vershalee Shukla, MD, Vincere Cancer Center
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
July 18, 2023
Primary Completion (Estimated)
December 31, 2033
Study Completion (Estimated)
December 31, 2038
Study Registration Dates
First Submitted
July 12, 2023
First Submitted That Met QC Criteria
July 12, 2023
First Posted (Actual)
July 20, 2023
Study Record Updates
Last Update Posted (Actual)
December 7, 2023
Last Update Submitted That Met QC Criteria
December 6, 2023
Last Verified
December 1, 2023
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- VCC-BIOBANK-001
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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