Clin2
NCT06538181Possibly a fitRecruiting

Testing pacritinib for VEXAS syndrome

E1 Ubiqutin-activating Enzyme, X-linked, Autoinflammatory, Somatic SyndromeVEXASVexas Syndrome

Treatments studied

Part of Blood & lymphatic, Genetic & congenital, Immune system & allergy clinical trials.

This trial tests a new drug called pacritinib for people with VEXAS syndrome, a rare autoinflammatory condition. The goal is to see if pacritinib can help control symptoms like rashes, joint pain, and low blood counts.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 1
Enrollment
15 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You must have a confirmed UBA1 gene mutation (the one that causes VEXAS syndrome).
  • You must have had at least one VEXAS symptom in the past or present, such as a rash, joint pain, fever, or low blood counts.
  • You can have tried a JAK inhibitor before, but if you did, it must not have worked well enough, and you need to stop it for at least 28 days before starting this trial.
  • Your steroid dose (like prednisone) must be stable for at least 14 days before you start the study drug.
  • You must be 18 or older and have adequate organ function (kidneys, liver, blood counts).

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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