RecruitingPhase 2NCT06782373

A Study to Assess the Effectiveness and Safety of Pacritinib in Patients With VEXAS Syndrome (PAXIS)

Studying VEXAS syndrome

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Key facts

Sponsor
Swedish Orphan Biovitrum
Principal Investigator
Study Physician
Sobi, Inc.
Intervention
Pacritinib(drug)
Enrollment
78 enrolled
Eligibility
18 years · All sexes
Timeline
20252026

Study locations (20)

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT06782373 on ClinicalTrials.gov

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