Patient-Derived Xenografts to Reduce Cancer Health Disparities
University of California Minority Patient-Derived Xenograft (PDX) Development and Trial Center (UCaMP) to Reduce Cancer Health Disparities
Who can join
As published by the study on ClinicalTrials.gov. "Not stated" means the study hasn't said — ask the study team.
- Age
- 21 Years to 100 Years
- Sex
- All sexes
- Healthy volunteers
- Not accepted
- Compensation
- Not stated
Other requirements are listed under Eligibility below. Only the study team can confirm whether you can join.
What to expect
No one can promise a trial will help you personally — that is what the research is trying to find out.
What participation involves
- Procedures mentioned: Biopsies, Urine samples
Only what the study's summary and detailed description on ClinicalTrials.gov say. Time periods may describe the whole study or a part of it — ask the study team what applies to you.
Show the study's own words
- "OUTLINE: Patients undergo collection of tumor tissue samples during standard of care tumor biopsy or surgical resection to establish PDXs."
- "Patients may also undergo collection of blood, saliva, and urine samples to compare deoxyribonucleic acid (DNA) abnormalities to noncancer cells in order to determine if they were present before the cancer started or developed with it."
- Compensation
- Not stated
- Study-related exams and procedures are typically provided at no cost. This is how many trials work in general — confirm the details for this study with the study team.
- Participants are monitored closely by the research team throughout the study.
- Some participants may receive access to an investigational treatment, which is still being studied.
- Your participation helps researchers learn whether this approach could help future patients.
About this study
In plain language
This study uses cancer samples from patients to grow tumors in animals. Researchers study differences in genes and treatment response to help improve cancer care for racial and ethnic minority groups. It is for adults receiving treatment for bladder, lung, stomach, or liver cancer.
This trial establishes patient-derived cancer xenografts in addressing cancer health and treatment disparities that disproportionately affect racial/ethnic minorities. Understanding the genetic and response differences among racial/ethnic minorities may help researchers enhance the precision of therapeutic treatments.
Compensation is read from the study's own description and may be missing — always confirm with the study team.
Eligibility
Who can join
- You are receiving treatment for bladder, lung, stomach, or liver cancer.
- You sign a consent form agreeing to join the study, which is kept on file.
Who can't join
- You have not given consent to join the study.
- Your sample is damaged or cannot be used.
- You are not yet an adult.
- You are pregnant.
- You are a prisoner.
- You are an adult who cannot give consent.
Simplified for readability. The official criteria below are what the study team uses.
Official eligibility criteria
Inclusion Criteria: * Patient receiving treatment for the above 4 cancers (bladder cancer, lung cancer, gastric/stomach cancer, and liver cancer) * Signed informed consent that will be put on file Exclusion Criteria: * No informed consent obtained * Specimen unacceptable/degraded/etc. * Individuals who are not yet adults (infants, children, teenagers) * Pregnant women * Prisoners * Adults unable to consent
Study sites (2)
CA
- UC Irvine Health/Chao Family Comprehensive Cancer Center · Orange, CA 92868Marian Waterman · Study contact · 949-824-2885 · marian.waterman@uci.eduMarian Waterman · Principal investigatorMore trials in Orange
- University of California Davis Comprehensive Cancer Center · Sacramento, CA 95817Luis G. Carvajal-Carmona · Study contact · 530-752-9654 · lgcarvajal@ucdavis.eduLuis G. Carvajal-Carmona · Principal investigatorMore trials in Sacramento