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Clinical Trials/NCT05499091
NCT05499091
Recruiting
Not Applicable

Functional Study to Indentify Genetic Etiology of Rare Diseases - ORIGIN

University Hospital, Angers1 site in 1 country1,200 target enrollmentOctober 10, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Rare Diseases
Sponsor
University Hospital, Angers
Enrollment
1200
Locations
1
Primary Endpoint
Identification of at least 80 new genes implicated in rare diseases via high-throughput sequencing technics and through functional studies.
Status
Recruiting
Last Updated
9 months ago

Overview

Brief Summary

Next generation sequencing (NGS) allows some better diagnostic results, particularly, in the rare diseases field. At a twenty five percent rate, those exams highlight some variants which are not yet described in human pathology. The relationship between a variant found inside a candidate gene and a pathology, is able to be confirmed by functional studies at a protein level. This study aims to build a biological collection to feed further functional studies to confirm the relationship between NGS identified variants, and the clinical signs and symptoms.

Registry
clinicaltrials.gov
Start Date
October 10, 2022
End Date
October 10, 2045
Last Updated
9 months ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
University Hospital, Angers
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Child or adult affected by a rare disease whose molecular functions are not known, or whose pathophysiologic mechanism are not fully understood.
  • Patient included inside the BaMaRa (French rare disease national data bank) database dedicated to the rare diseases.
  • Patient Affiliated to the French social security system.
  • Patient consent form or legal representative consent form obtained.
  • Patient's parent :
  • Parent of a patient affected by a rare disease whose molecular functions are not known, or whose pathophysiologic mechanism are not fully understood.
  • Parent included in the BaMaRa database.
  • Parent affiliated to the French social security system.
  • Parent consent form obtained for himself/herself.
  • Patient's brother or sister :

Exclusion Criteria

  • Poor understanding of the French language
  • Legal of administrative liberty deprivation
  • Psychiatric force care

Outcomes

Primary Outcomes

Identification of at least 80 new genes implicated in rare diseases via high-throughput sequencing technics and through functional studies.

Time Frame: 23 years

Candidate genes, suspected to be responsible for rare diseases will be identified before the inclusion, during standard medical care, by exome or genome sequencing.

Collecting biological samples to build up a biobank

Time Frame: 23 years

After a candidat gene identification, patient will be proposed sampling (blood or urine) or if a skin biopsy, an amniotic fluid puncture or any surgery are done during standard care, the remaing tissue or fluid, or operative wastes will be eligible too, to be stored in the biobank.

Candidat gene validation through functional studies.

Time Frame: 23 years

Biological samples from the biobank will be made available after the study, to some specialized research teams, in order to validate or overturn those previously gene candidates by the way of some biological technics.

Study Sites (1)

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