Clin2
NCT06782373Possibly a fitActive, not recruiting

Pacritinib for treating VEXAS syndrome

VEXASVEXAS Syndrome

Treatments studied

Part of Blood & lymphatic, Cancer clinical trials.

This trial tests a drug called pacritinib for people with VEXAS syndrome. It aims to see if pacritinib can help control inflammation and reduce the need for steroids. You may qualify if you have a specific UBA1 gene mutation and are currently on a stable steroid dose.

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

Phase
Phase 2
Enrollment
78 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You must have a confirmed change (mutation) in the UBA1 gene at a specific spot called M41 or nearby.
  • You must have had inflammation in at least one organ system (like skin, joints, eyes, or lungs) due to VEXAS in the past 6 months.
  • You need to be taking a stable dose of prednisone or prednisolone (15 to 45 mg every day).
  • You should be able to do most daily activities on your own (Karnofsky score of 50% or more).
  • Your liver, kidney, and blood cell counts must meet certain safe levels (checked by blood tests).
  • You cannot have had a stem cell or organ transplant, more than one ICU stay for VEXAS in 6 months, or certain other conditions.

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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