BE.Amycon Biobank & Data Registry UZ Leuven
BE.Amycon Biobank & Data Registry UZ Leuven: Human Body Material (HBM) Collection and Data Collection of Patients With Amyloidosis
- Amyloidosis
- AL Amyloidosis
- Amyloidosis Cardiac
At a glance
- Phase
- Phase not stated
- Study type
- Observational
- Sponsor
- Universitaire Ziekenhuizen KU Leuven
- Enrolment target
- 505
- Started
- 24 September 2025
- Main results due
- September 2029
- Study sites
- 2
- Registry updated
- 25 September 2026
Can you take part?
- Aged 18 years and over.
- Open to any sex.
- Healthy volunteers can take part.
These are the headline rules only. Every study has a longer list, and whether you are eligible is decided by the research team at the site — never by this page.
Read the full eligibility criteria
Inclusion Criteria: * Provide consent and sign informed consent form * Age 18 years or older * Diagnosis of amyloidosis (suspected or confirmed, any subtypes) * For the prospective sample collection only: newly diagnosed (any subtype) or at relapse (AL amyloidosis) Exclusion Criteria: * Not willing to sign informed consent * Not able to sign informed consent
What this study is about
In the sponsor’s own words, from the registry.
The goal of this study is to collect and store human body material (HBM) of patients with amyloidosis in a biobank "BE.Amycon biobank" for future research and to collect clinical data of patients with amyloidosis in a database "BE.Amycon data registry".
Study sites(2)
UZ Leuven Gasthuisberg - hematology
Leuven, Belgium
Recruiting
UZ Leuven Gasthuisberg - cardiology
Leuven, Belgium
Recruiting
Showing 2 of 2 sites. 2 of the 2 sites on this study are recruiting right now — a site can stop enrolling while the study as a whole is still open.
Source: ClinicalTrials.gov record NCT07172243. Trialion does not run this study, is not paid to refer anyone to it, and cannot enrol you. Eligibility is always decided by the research team at the site.
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