A program to collect cancer-related samples and data for better cancer care

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This program aims to enhance cancer care by creating a comprehensive repository of biological samples and associated data from patients diagnosed with cancer or at risk of developing it. Participants will provide blood, tissue, and other biological samples, along with survey responses and medical records, to support ongoing cancer research and personalized medicine initiatives. The data collected will be utilized to facilitate new clinical trials and improve cancer treatment standards through collaboration with various healthcare providers. This is an observational study, meaning it does not involve any treatment interventions.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* 18 years of age and older.
* Has a diagnosis of cancer or is suspected of having cancer.
* Able to understand and sign the Informed Consent form directly.
* Pregnant women are permitted to be enrolled.

Exclusion Criteria:

* Prisoners

Where it's running

• University of New Mexico Comprehensive Cancer Center
  Albuquerque, New Mexico, United States Recruiting

Study contacts

• Principal investigator: Leslie Andritsos, MD — University of New Mexico Cancer Center
• Study coordinator: Ellen Wojcik, MBA-HCM
• Email: ewojcik@salud.unm.edu
• Phone: 505 272-4946

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.