RECRUITING

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

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

A Phase 1 Study of Repeat PET/CT Imaging in People With CAPS and Anakinra-Induced Amyloidosis Using Amyloid-Reactive Peptide 124I-AT-01 (124I-p5+14, Iodine-124I-Evuzamitide) to Measure Changes in Organ-Specific Amyloid Load

Quick Facts

Study Start:2025-05-21
Study Completion:2032-01-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06974877

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 120 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Aged 18 years and older.
  2. 2. Currently enrolled on NIH protocol 17-I-0016 with a documented diagnosis of MWS or NOMID.
  3. 3. 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.
  4. 4. Developed skin thickening at the site of anakinra injection.
  5. 5. Participants who can become pregnant or who can impregnate their partner must agree to use 2 highly effective methods of contraception, at least 1 of which must be a barrier method, when engaging in sexual activities that can result in pregnancy, beginning 28 days prior to baseline until 90 days after the last PET/CT scan. Acceptable methods of contraception include the following:
  6. 1. Barrier methods:
  7. * External or internal condom with spermicide.
  8. * Diaphragm or cervical cap with a spermicide.
  9. 2. Non-barrier methods:
  10. * Hormonal contraception.
  11. * Intrauterine device.
  12. * Hysterectomy, oophorectomy, or tubal ligation in women
  13. * Vasectomy in men
  14. 3. Other.
  1. 1. Known hypersensitivity to 124I-AT-01, AT-01, or any of their excipients.
  2. 2. Known hypersensitivity to KI.
  3. 3. Pregnant or breastfeeding.
  4. 4. Currently receiving dialysis.
  5. 5. Currently taking heparin or heparin derivatives (eg, low molecular weight heparins) or other blood thinners for anticoagulation.
  6. 6. Any condition that, in the opinion of the study team, contraindicates participation in this study.

Contacts and Locations

Study Contact

Sara Alehashemi, M.D.
CONTACT
(301) 761-7570
sara.alehashemi@nih.gov

Principal Investigator

Sara Alehashemi, M.D.
PRINCIPAL_INVESTIGATOR
National Institute of Allergy and Infectious Diseases (NIAID)

Study Locations (Sites)

National Institutes of Health Clinical Center
Bethesda, Maryland, 20892
United States

Collaborators and Investigators

Sponsor: National Institute of Allergy and Infectious Diseases (NIAID)

  • Sara Alehashemi, M.D., PRINCIPAL_INVESTIGATOR, National Institute of Allergy and Infectious Diseases (NIAID)

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-05-21
Study Completion Date2032-01-31

Study Record Updates

Study Start Date2025-05-21
Study Completion Date2032-01-31

Terms related to this study

Keywords Provided by Researchers

  • Muckle-Wells Syndrome
  • Neonatal Onset Multisystem Inflammatory Disease
  • Interleukin 1 Receptor Antagonist Protein
  • Anakinra
  • AMYLOIDOSIS
  • AIL1RAP

Additional Relevant MeSH Terms

  • Cryopyrin-Associated Periodic Syndromes
  • Amyloidosis