Could genome sequencing at birth spot rare diseases sooner? french study launches

NCT ID NCT06875089

Recruiting now Knowledge-focused Sponsor: Centre Hospitalier Universitaire Dijon Source: ClinicalTrials.gov ↗

First seen Nov 21, 2025 · Last updated May 01, 2026 · Updated 24 times

Summary

This study will test if it's possible and acceptable to screen newborns for rare diseases using genome sequencing. About 5,000 newborns in France will take part. The goal is to see if this method can quickly find treatable or actionable rare diseases, helping doctors start care earlier.

Disclaimer Read more

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 NEWBORN SCREENING PROGRAMMES FOR RARE DISEASES are added.

Our safety recommendation!

By submitting, you agree to our Terms of use

Contacts and locations

Show contact details

Study contacts

Contact

Phone: •••-•••-•••• Email: •••••@•••••

Locations

CHU Besançon
NOT_YET_RECRUITING

Besançon, 25000, France

Contact Phone: •••-•••-•••• Email: •••••@•••••
CHU Dijon Bourgogne
RECRUITING

Dijon, 21000, France

Contact Phone: •••-•••-•••• Email: •••••@•••••
CHU Hôtel Dieu
NOT_YET_RECRUITING

Nantes, 44093, France

Contact Phone: •••-•••-•••• Email: •••••@•••••
CHU Rennes - Hôpital Sud
NOT_YET_RECRUITING

Rennes, 35203, France

Contact Phone: •••-•••-•••• Email: •••••@•••••
CHU d'Angers
NOT_YET_RECRUITING

Angers, 49933, France

Contact Phone: •••-•••-•••• Email: •••••@•••••

Conditions

Explore the condition pages connected to this study.

NEWBORN SCREENING PROGRAMMES FOR RARE DISEASES NEWBORN SCREENING PROGRAMMES FOR RARE DISEASES