Protocol Details

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

This study is currently recruiting participants.

Summary | Eligibility | Citations | Contacts

Summary

Number

001867-I

Sponsoring Institute

National Institute of Allergy and Infectious Diseases (NIAID)

Recruitment Detail

Type: Participants currently recruited/enrolled
Gender: Male & Female
Min Age: 18 Years
Max Age: 120 Years

Referral Letter Required

Yes

Population Exclusion(s)

Neonates;
Pregnant Women;
Children

Keywords

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

Recruitment Keyword(s)

None

Condition(s)

Cryopyrin-Associated Periodic Syndromes;
Amyloidosis

Investigational Drug(s)

Iodine I[124] Evuzamitide

Investigational Device(s)

None

Intervention(s)

Drug: 124I AT-01

Supporting Site

National Institute of Allergy and Infectious Diseases

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

INCLUSION CRITERIA:

An individual must meet all the following criteria to be eligible for this study:

1. Aged 18 years and older.

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

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. Developed skin thickening at the site of anakinra injection.

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:

a. Barrier methods:

-External or internal condom with spermicide.

-Diaphragm or cervical cap with a spermicide.

b.Non-barrier methods:

-Hormonal contraception.

-Intrauterine device.

-Hysterectomy, oophorectomy, or tubal ligation in women

-Vasectomy in men

c. Other.

EXCLUSION CRITERIA:

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

2. Known hypersensitivity to KI.

3. Pregnant or breastfeeding.

4. Currently receiving dialysis.

5. Currently taking heparin or heparin derivatives (eg, low molecular weight heparins) or other blood thinners for anticoagulation.

6. Any condition that, in the opinion of the study team, contraindicates participation in this study.


Citations:

Alehashemi S, Dasari S, Metpally A, Uss K, Castelo-Soccio LA, Heller T, Kellman P, Chen MY, Ahlman M, Kim J, Wargo S, Kuhns DB, Fink D, de Jesus A, Martin PS, Chang R, Bolanos J, Lee CR, Nasr SH, Goldbach-Mansky R, McPhail E. Anakinra-Associated Systemic Amyloidosis. Arthritis Rheumatol. 2024 Jan;76(1):100-106. doi: 10.1002/art.42664. Epub 2023 Nov 29. PMID: 37488949; PMCID: PMC10805950.

Nasr SH, Alehashemi S, Dasari S, Waldman M, Afzali B, Chiu A, Bolanos J, Goldbach-Mansky R, McPhail ED. Anakinra-associated renal amyloidosis. Kidney Int. 2024 Feb;105(2):395-396. doi: 10.1016/j.kint.2023.08.020. PMID: 38245224; PMCID: PMC10827346.

Alehashemi S, Dasari S, de Jesus AA, Cowen EW, Lee CR, Goldbach-Mansky R, McPhail ED. Anakinra-Associated Amyloidosis. JAMA Dermatol. 2022 Dec 1;158(12):1454-1457. doi: 10.1001/jamadermatol.2022.2124. PMID: 36223107.

Contacts:

Principal Investigator

Referral Contact

For more information:

Sara Alehashemi, M.D.
National Institute of Allergy and Infectious Diseases (NIAID)
NIHBC 10 - CLINICAL CENTER BG RM 11C215
10 CENTER DR
BETHESDA MD 20892
(301) 761-7570
sara.alehashemi@nih.gov
Sara Alehashemi, M.D.
National Institute of Allergy and Infectious Diseases (NIAID)
NIHBC 10 - CLINICAL CENTER BG RM 11C215
10 CENTER DR
BETHESDA MD 20892
(301) 761-7570
sara.alehashemi@nih.gov
Office of Patient Recruitment
National Institutes of Health Clinical Center (CC)
Building 61, 10 Cloister Court
Bethesda, Maryland 20892
Toll Free: 1-800-411-1222
Local Phone: 301-451-4383
TTY: TTY Users Dial 7-1-1
ccopr@nih.gov

Clinical Trials Number:

NCT06974877
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