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Clinical Trial Summary

This study is being done to learn more about how changes in certain genes may be linked to cancer. Some people with cancer got their disease because they inherited an abnormal (mutated) gene. The researchers of this study want to better understand the risks that are linked to genetic changes in these less well-studied genes. By understanding these risks, we believe that doctors will be able to give better advice to families with mutations in these genes.


Clinical Trial Description

PROMPT (Prospective Registry of Multiplex Testing) is an Internet-based, patient-directed ascertainment study. It is a partnership between Memorial Sloan Kettering, University of Pennsylvania, Mayo Clinic, and Dana Farber Cancer Institute in collaboration with Ambry Genetics, GeneDx, Myriad Genetics, Pathway Genomics, and Quest Laboratories (5 laboratories providing multiplex panel testing commercially). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02665195
Study type Observational [Patient Registry]
Source Memorial Sloan Kettering Cancer Center
Contact
Status Active, not recruiting
Phase
Start date January 2016
Completion date January 2025

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