Actively Recruiting

Age: 18Years +
All Genders
ID06377462

Multicenter, Interdisciplinary National VEXAS Registry With Accompanying Biomaterial Collection

Led by Technische Universität Dresden · Updated on 2026-05-15

500

Participants Needed

17

Research Sites

52 weeks

Total Duration

On this page

Sponsors

T

Technische Universität Dresden

Lead Sponsor

B

Bristol-Myers Squibb

Collaborating Sponsor

AI-Summary

What this Trial Is About

This research aims to rapidly gather real-world information about VEXAS syndrome, focusing on its epidemiology, treatments, and disease progression during standard medical care. It also collects biomaterials to study links between genetic makeup and symptoms, to find the best treatment plans, and to identify key diagnostic features and biomarkers. The study is observational, involving patients with confirmed or suspected VEXAS syndrome aged 18 or older who provide consent. There are no assigned treatments or interventions as it records information during routine clinical practice. The registry collects data and biospecimens over a period of up to five years to support detailed analysis. Participants will provide clinical data, treatment histories, and quality of life information through questionnaires and laboratory tests. Researchers will monitor disease manifestations, treatments, and clinical outcomes, as well as collect biosamples for translational research. The study follows participants for up to five years to better understand VEXAS syndrome and its management.

CONDITIONS

Brief Title

Multicenter, Interdisciplinary National VEXAS Registry With Accompanying Biomaterial Collection

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with established or suspected (clinical and hematological criteria) VEXAS Syndrome
  • Age 65 18 years
  • Signed informed consent form
Not Eligible

You will not qualify if you...

  • Patients who are not in a position to understand the nature and scope of participation in this register

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Long-term Monitoring

Duration - Up to 5 years

Participants are observed over time to collect epidemiological data, monitor disease manifestations, document treatments, and analyze clinical outcomes.

Periodic visits over 5 years

Trial Site Locations

Total: 17 locations

1

Universitätsklinikum Aachen

Aachen, Germany

Actively Recruiting

2

Klinikum Chemnitz gGmbH

Chemnitz, Germany

Actively Recruiting

3

Universitätsklinikum Carl Gustav Carus

Dresden, Germany, 01307

Actively Recruiting

4

Universitätsklinikum Düsseldorf

Düsseldorf, Germany

Actively Recruiting

5

Evang. Kliniken Essen-Mitte

Essen, Germany

Actively Recruiting

6

Universitätsmedizin Göttingen

Göttingen, Germany

Actively Recruiting

7

Universitätsklinikum Hamburg-Eppendorf

Hamburg, Germany

Actively Recruiting

8

Universitätsklinikum Jena

Jena, Germany

Actively Recruiting

9

Universitätsklinikum Leipzig AöR

Leipzig, Germany

Actively Recruiting

10

Universitätsmedizin Mannheim

Mannheim, Germany

Actively Recruiting

11

Klinikum rechts der Isar TUM

München, Germany

Actively Recruiting

12

Klinikum Nürnberg, Campus Nord

Nuremberg, Germany

Actively Recruiting

13

Klinikum Osnabrück GmbH

Osnabrück, Germany

Actively Recruiting

14

Helios Kliniken Schwerin GmbH

Schwerin, Germany

Actively Recruiting

15

Robert Bosch Gesellschaft für Medizinische Forschung mb

Stuttgart, Germany

Actively Recruiting

16

Krankenhaus der Barmherzigen Brüder

Trier, Germany

Actively Recruiting

17

Universitätsklinikum Tübingen

Tübingen, Germany

Actively Recruiting

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Research Team

K

Katja Sockel, Dr. med.

K

Katharina Goetze, Prof.

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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