Registry for evaluating the Precision Medicine Molecular Tumor Board

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 observational study aims to assess the clinical utility of the Precision Medicine Molecular Tumor Board (PMMTB) by tracking patient outcomes related to hematologic and solid neoplasms. Participants will undergo genetic testing of their tumors, and the study will evaluate how the insights gained from the PMMTB can inform treatment decisions. The study is designed to gather data that may enhance personalized medicine approaches in oncology.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Clinically suspected or histologically confirmed solid or hematological malignancy
* Undergoing genetic testing of tumor
* Ability to understand written informed consent document
* Willingness to sign written informed consent document

Exclusion Criteria:

* Pediatric patients (age\<18 years) will be excluded due to a lack of expertise on the molecular tumor committee

Where it's running

• University of Wisconsin Carbone Cancer Center
  Madison, Wisconsin, United States Recruiting

Study contacts

• Principal investigator: Dustin Deming, MD — University of Wisconsin, Madison
• Study coordinator: Cancer Connect
• Email: clinicaltrials@cancer.wisc.edu
• Phone: 8006228922

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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.