Multicenter, Interdisciplinary National VEXAS Registry With Accompanying Biomaterial Collection

Recruiting now

Conditions studied: VEXAS Syndrome

In brief

The aim is rapid collection of real-life data on the epidemiology, treatment and disease course in patients with VEXAS syndrome during routine clinical practice and collect biomaterials to evaluate genotype-phenotype associations, determine optimal treatment schedule, identify diagnostic features and biomarkers

Key facts

Study ID
NCT06377462
Run by
Technische Universität Dresden
People needed
500
Starts
2024-03-13
Expected to finish
2030-12-31
Last updated by the study team
2026-05-15

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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