Repeat PET/CT Imaging in People With CAPS and Anakinra-Induced Amyloidosis Using an Amyloid-Reactive Peptide to Measure Changes in Organ-Specific Amyloid Load

Trial statusRecruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexAll
Age18-120
SponsorNational Institute of Allergy and Infectious Diseases (NIAID)

About this trial

Background:

Anakinra is a drug used to treat people with certain diseases that affect their immune systems. Sometimes anakinra can cause proteins under the skin to clump together. These clumps are called amyloidosis; they can spread to other organs. The only way to diagnose amyloidosis is to remove a piece of tissue (biopsy). Researchers want to find a way to locate amyloidosis in internal organs using positron emission tomography (PET)/computed tomography (CT).

Objective:

To test a new tracer used during PET/CT scans in people with amyloidosis. A tracer is a radioactive dye injected into the body.

Eligibility:

Adults aged 18 years or older with amyloidosis from anakinra injections. They must be enrolled in NIH protocol 17-I-0016.

Design:

Participants will come to the clinic once every 6 months for 2 years. Each visit will be 1 day.

They will have a PET/CT scan with the new tracer at each visit: The tracer will be given through a tube attached to a needle inserted into a vein.

The PET/CT scanner is a machine shaped like a doughnut. Participants will lie still on a padded table. The table will move in and out of the machine. The scan takes about 1 hour.

Radiation from the tracer will remain in the body for 24 hours after each scan. Participants will need to follow rules to avoid exposing pets and other people.

Participants will collect a 24-hour urine sample before each visit. They will also have blood tests and a physical exam at each visit.

Participants will receive a follow-up phone call about 1 week after each visit.

Eligibility criteria

Qualifiers

Aged 18 years and older.

Currently enrolled on NIH protocol 17-I-0016 with a documented diagnosis of MWS or NOMID.

Agree to allow data collected in this study to be shared with and stored on NIH protocol 17-I-0016 for that study s research analyses.

Developed skin thickening at the site of anakinra injection.

Disqualifiers

Known hypersensitivity to 124I-AT-01, AT-01, or any of their excipients.

Known hypersensitivity to KI.

Pregnant or breastfeeding.

Currently receiving dialysis.

Trial design

Treatments tested in this trial

  • 124I AT-01

Treatment groups

30 Participants
are divided into 1 treatment group