# Clinical Phenotype and Prevalence of VEXAS Syndrome in Internal Medicine

> **NCT07708688** · — · NOT_YET_RECRUITING · sponsor: **Centre Hospitalier Universitaire Vaudois** · enrollment: 50 (estimated)

## Conditions studied

- Vexas Syndrome

## Interventions

- **DIAGNOSTIC_TEST:** UBA1 Genetic Testing

## Key facts

- **NCT ID:** NCT07708688
- **Lead sponsor:** Centre Hospitalier Universitaire Vaudois
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** NOT_YET_RECRUITING
- **Start date:** 2026-07
- **Primary completion:** 2028-06
- **Final completion:** 2028-06
- **Target enrollment:** 50 (ESTIMATED)
- **Last updated:** 2026-07-16

## Collaborators

- [object Object]
- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT07708688

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT07708688, "Clinical Phenotype and Prevalence of VEXAS Syndrome in Internal Medicine". Retrieved via MORVS 2026-10-20 from https://api.morvs.ai/clinical/NCT07708688. Licensed CC0.

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