Collection of biospecimens for cancer research
Vincere Biobank Research Protocol
This study is collecting blood, urine, and tissue samples from people to help researchers find better ways to screen for and treat cancer.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 5000 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Vincere Cancer Center Academic / other |
| Locations | 1 site (Scottsdale, Arizona) |
| Trial ID | NCT05954299 on ClinicalTrials.gov |
What this trial studies
The Vincere Biobank is designed to collect high-quality biospecimens and associated clinical data to support research aimed at improving cancer screening, treatment, and patient care. Participants will provide samples such as blood, urine, and tissue, which will be stored for future studies. This observational approach allows researchers to access valuable resources that can lead to advancements in cancer medicine.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18 and older who are willing to donate biospecimens and provide informed consent.
Not a fit: Patients who are minors or unable to give informed consent will not benefit from this study.
Why it matters
Potential benefit: If successful, this initiative could enhance the understanding of cancer and lead to improved diagnostic and treatment options for patients.
How similar studies have performed: Other biobank studies have shown success in advancing cancer research, making this approach a well-established method in the field.
Eligibility criteria
Show full inclusion / exclusion 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
Where this trial is running
Scottsdale, Arizona
- Vincere Cancer Center — Scottsdale, Arizona, United States (Recruiting)
Study contacts
- Principal investigator: Vershalee Shukla, MD — Vincere Cancer Center
- Study coordinator: Christine Lau, MD
- Email: drlau@vincerecancer.com
- Phone: 480-306-5390
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.