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Characterization of Phenotype and Genotype of Early Onset Enteropathies (IMMUNOBIOTA)

I

Imagine Institute

Status

Enrolling

Conditions

Inflammatory Bowel Disease

Treatments

Other: Biological sampling

Study type

Observational

Funder types

Other

Identifiers

NCT02614911
IMIS2014-01

Details and patient eligibility

About

This study has been set up in order to characterize phenotypes and genotypes of patients with early onset enteropathies.

In that goal, Investigators will collect biological samples (mainly blood) of patients suffering from early onset enteropathies and their healthy relatives.

Full description

This study specifically aims at the genetic analysis of early onset enteropathies with the goal in mind to delineate human pathways necessary to maintain intestinal homeostasis despite the considerable density of microbes colonizing the distal part of the human intestine.

Enrollment

1,445 estimated patients

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Main Inclusion Criteria:

  • Severe chronic enteropathy
  • Patients developing their first symptoms within the first 6 years of life and, in priority within the first two years of life, or patients with a disease of later onset, in case of a familial history suggestive of inherited mutations notably in families comprising several affected members
  • OR : Be a patient's relative, even if presenting with enteropathy of later onset.

Main Exclusion Criteria:

  • Subject having participated to any therapeutical clinical study in the 30 days preceding the inclusion in this study,

Trial design

1,445 participants in 2 patient groups

Sick patients
Description:
Biological sampling of blood for all patients. Biological sampling of saliva, biopsies (skin and endoscopic), feces, for some patients
Treatment:
Other: Biological sampling
Healthy relatives
Description:
Biological sampling of blood for all healthy relatives
Treatment:
Other: Biological sampling

Trial contacts and locations

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Central trial contact

Nadine Cerf-Bensussan; Fabienne Charbit-Henrion

Data sourced from clinicaltrials.gov

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