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NCT04006535: FAMILYVASC

Whole Exome Sequencing of Familial and Pediatric Forms of Vasculitis

Recruiting now Last updated 8 July 2019
What this trial tests

trial testing genetic analysis in Vasculitis in 100 participants. Currently enrolling.

Timeline
1 June 2019
Primary endpoint
1 June 2029
1 June 2029

Quick facts

Lead sponsorBenjamin Terrier
StatusRecruiting now
Study typeOBSERVATIONAL
Enrollment100
Start date1 June 2019
Primary completion1 June 2029
Estimated completion1 June 2029
Sites1 location across France

Drugs / interventions tested

Conditions studied

Sponsor

Benjamin Terrier

Who can join

Eligibility, any sex, with Vasculitis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The FAMILYVASC study is a prospective observational study which will aim to identify susceptibility loci and genes for systemic vasculitis risk in patients with familial or pediatric forms of vasculitis. Genetic analysis based on whole exome sequencing will be carried out through salivary DNA.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of genetic analysis

Trials testing the same drug.

Other recruiting trials for Vasculitis

Currently open trials in the same condition.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04006535.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing