Rare bone cancer study seeks DNA clues from patients
NCT ID NCT01200680
First seen Nov 01, 2025 · Last updated Jun 15, 2026 · Updated 30 times
Summary
This study aims to find genetic changes linked to chordoma, a rare and serious bone cancer. Researchers will collect saliva and medical history from 188 people in the U.S. or Canada who have chordoma but no family history of it. The goal is to learn how often certain gene alterations occur in sporadic chordoma patients.
Disclaimer
Read more
Show less
This is a summary of
the original study
.
Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for GENES are added.
By submitting, you agree to our Terms of use
Contacts and locations
Show contact details
Enter your email to view the contact information for this study.
By submitting, you agree to our Terms of use
Locations
-
Westat, Inc.
Rockville, Maryland, 20850, United States
Conditions
Explore the condition pages connected to this study.