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2024-517942-33-03RecruitingPhase 3

A multi-center phase 3 study of 18F-florbetaben positron emission tomography/computed tomography (PET-CT) to non-invasively diagnose cardiac AL amyloidosis: the PETAL study.

Source: EU CTIS (euclinicaltrials.eu) · Last updated 21 Jan 2025 · Not updated for over 12 months - ask the site whether it is still open

Next steps

Brief summary (registry, in English)

To define the concordance (with 95% confidence interval) of two pathways for the diagnosis of AL-CA in patients with a monoclonal component: the traditional (invasive) pathway and a non-invasive pathway using PET/CT with 18F-florbetaben ( visual assessment)

Status (registry)
Recruiting
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
150 (estimated)
First submitted
18 Nov 2024
Start date
4 Feb 2023
Lead sponsor
Fondazione Toscana Gabriele Monasterio
Diseases
Amyloidosis
EU CT number
2024-517942-33-03
EudraCT number
2022-002585-33

What you commit to

  • Study type: Interventional · Phase 3
  • Planned participants: 150
  • 6 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of EU CTIS (euclinicaltrials.eu). It describes the study design.

AI-kivonat: who the study is looking for

Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for adults with signs that suggest cardiac amyloidosis (a heart disease caused by protein build-up). It tests whether a PET-CT scan with 18F-florbetaben can diagnose cardiac AL amyloidosis without invasive tests.

Age
Older than 18 years
Sex
Men and women
Disease stage
Signs that doctors judge compatible with cardiac amyloidosis: raised NT-proBNP (>332 ng/L, without kidney failure or atrial fibrillation) or BNP >81 ng/L, or a thick heart wall (>12 mm on echocardiogram), or a typical pattern on heart MRI.
Earlier treatment
Must not have joined a trial with an experimental drug within 30 days before screening or 5 half-lives of the study drug, whichever is longer.

Main reasons for not taking part

  • Allergy to the active substance or an ingredient of Neuraceq
  • Chronic kidney disease (eGFR <30 mL/min/1,73 m2)
  • Liver disease with raised liver tests
  • Pregnancy or breastfeeding
  • Cannot lie flat for about 60 minutes

Read by machine on 9 Nov 2026.

Who cannot take part

Copied verbatim from EU CTIS (euclinicaltrials.eu) and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Participation to a study involving the administration of an experimental drug within 30 days from the screening or 5 half-lives of the study drug, whichever the longest

Other illness

  • Hypersensitivity to the active principle or any excipient listed in the paragraph 6.1 of the Summary of Product Characteristics (RCP) of Neuraceq®
  • Chronic kidney disease (estimated glomerular filtration rate <30 mL/min/1,73 m2)
  • New York Heart Association (NYHA) class IV

Lab values

  • Liver disease [elevation >2 times above the upper reference limit of AST (normal range: males 34 UI/L, females 30 UI/ L), ALT (normal range: males 40 UI/L, females 35 UI/L), gamma-GT (normal range: 64 UI/L)
  • Pregnancy or breastfeeding, women with childbearing potential and sexually active not employing highly effective contraceptive methods with a low dependency on the user (from the screening to the end of visit 1), which include: i. abstinence, ii. sexual intercourse only with same-sex partners, iii. monogamous relationship with a partner with prior vasectomy, iv. intrauterine device, v. combined hormonal contraception including estrogens and progesteron-like hormones plus the inhibition of ovulation (oral, intravaginal or transdermal), vi. hormonal contraception based on progesterone- like compounds plus the inhibition of ovulation (oral, injectable, implantable), viii. intrauterine device with hormone release. The highly effective contraceptive measures above are not required for women made sterile by surgical means (for example through tube ligation, hysterectomy, bilateral salpingectomy, bilateral ovariectomy) or after the menopause, defined as 12 months of spontaneous amenorrhea without another clinical cause and with elevated FSH levels in agreement with the expected values for the menopause. For patients with true abstinence or with just same-sex partners, contraception is not required, as far as this is in line with their preferred and habitual lifestyle. Periodical abstinence (for example, estimate of the timing of ovulation or assessment of body temperature) and coitus interruptus are not acceptable contraceptive methods. If a patient stops to be abstinent, she must use the highly effective contraceptive methods above. The pregnancy status in women potentially fertile will be checked through the measurement of beta human gonadotropin on the serum and repeated at the end of the study

Other

  • Performing a PET/CT or scintigraphic exam within 24 hours
  • Impossibility to lay flat for about 60 minutes
  • Lack of informed consent or impossibility to complete study procedures

Who the study is looking for

  • Men and women aged >18 years
  • Ability to understand, sign and date the informed consent
  • NT-proBNP values >332 ng/L in the absence of renal insufficiency or atrial fibrillation or left ventricular mean wall thickness >12 mm on echocardiogram and/or a pattern of circumferential or diffuse subendocardial late gadolinium enhancement and/or BNP >81 ng/L, in a clinical setting judged compatible with CA by experienced clinicians

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on EU CTIS (euclinicaltrials.eu)

Sites (6)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Azienda Socio Sanitaria Territoriale Papa Giovanni XXIIIBergamoItalyRecruiting
University Hospital Of FerraraFerraraItalyRecruiting
Azienda Ospedaliera dei ColliNaplesItalyRecruiting
Fondazione IRCCS Policlinico San MatteoPaviaItalyRecruiting
Fondazione Toscana Gabriele MonasterioPisaItalyRecruiting
Azienda Sanitaria Universitaria Giuliano IsontinaTriesteItalyRecruiting

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This page is information, not medical advice. Discuss any trial with your doctor.