About this trial

This is an exploratory natural history protocol that will enroll patients with known genetic diseases, such as VEXAS syndrome, or as yet undiagnosed disorders of inflammation with the goal of improving our understanding of disease processes. Blood, saliva, hair, nail, or buccal samples may be collected for genetic analysis, blood samples will be obtained for immunologic and other functional studies, and a small number of subjects may undergo skin biopsy.

Eligibility criteria

Qualifiers

Stated willingness to participate in study procedures (which at the very least includes providing a mail-in blood or saliva sample for genetic analysis);

Regardless of sex assigned at birth, at least one month of age;

A medical history that, in the expert opinion of the PI and study team, is consistent with the possibility of autoinflammatory disease or known diagnosis of an autoinflammatory disease, such as VEXAS syndrome; and

Ability of the subject, parents (in the case of children), or Legally Authorized Representative to understand and the willingness to sign a written informed consent document.

Disqualifiers

None

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

1,500 Participants
are grouped into 3 trial groups

Locations

2
NYC H+H/Bellevue10016, New YorkNew York, United States
NYU Langone Health10016, New YorkNew York, United States

Sponsors and collaborators

NYU Langone Health

Lead sponsor