Personalized cancer therapy assessment

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 study aims to investigate how personalized cancer therapy affects patient responses and side effects by analyzing medical records and treatment outcomes. It includes both retrospective and prospective components, examining molecular profiling results to understand the predictive value of genetic testing on treatment efficacy. Optional research tests on biological samples will help identify biomarkers that may indicate how patients respond to therapies. The study will evaluate various patient outcomes, including tumor response, treatment failure, survival rates, and toxicity levels.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Must be willing to provide informed consent, parent permission, or assent

Exclusion Criteria:

* Subjects unable to give informed consent, parent permission, or assent

Where it's running

• UCSD Moores Cancer Center
  La Jolla, California, United States Recruiting
• Eisenhower Medical Center, Lucy Curci Cancer Center
  Rancho Mirage, California, United States Recruiting
• Rady Children's Hospital, San Diego
  San Diego, California, United States Recruiting

Study contacts

• Principal investigator: Shumei Kato, MD — University of California, San Diego
• Study coordinator: Lee Suzanna, MPH
• Email: sml012@health.ucsd.edu
• Phone: (858) 534-1306

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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.