Registry for diagnosing and managing AL amyloidosis in Europe
Official title: Bonding Molecular Genotyping and Phenotyping to Outcome Measures in AL Amyloidosis: A EUropean REgistry and Sample Sharing networK to Promote the Diagnosis and Management of Light Chain Amyloidosis (EUREKA)
Run by Fondazione IRCCS Policlinico San Matteo di Pavia · NCT06205953 · Data updated 2026-11-12
This study is creating a registry to help doctors better diagnose and manage AL amyloidosis in Europe by collecting patient information and samples to learn more about the disease.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years to 99 Years |
| Sex | All |
| Enrollment | 400 (estimated) |
| Sponsor | Fondazione IRCCS Policlinico San Matteo di Pavia Academic / other |
| Locations | 6 sites (Heidelberg and 5 other locations) |
| Status | Recruiting |
| Started | January 1, 2024 |
| Main results expected | June 1, 2026 |
| Study ends | June 1, 2026 |
| Registry record updated | April 16, 2026 |
| Trial ID | NCT06205953 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include adults aged 18 and older who have been newly diagnosed with systemic AL amyloidosis and are treatment-naïve.
✕Probably not a fit
Patients with non-AL amyloidosis or those who have previously received treatment for AL amyloidosis may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This initiative aims to create a comprehensive registry of new cases of AL amyloidosis across Europe, focusing on patients evaluated at referral centers. It will establish a biorepository and sample sharing network to investigate the disease mechanisms using advanced molecular technologies and big data analysis. The project seeks to enhance early diagnosis, understand the disease's natural history, and refine techniques for detecting minimal residual disease in patients who have responded to therapy.
Why it matters
Potential benefit: If successful, this project could lead to improved diagnosis and management strategies for patients with AL amyloidosis.
How similar studies have gone: Other studies utilizing registries and advanced molecular techniques have shown promise in improving outcomes for similar conditions, indicating a potential for success in this approach.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * diagnosis of systemic AL amyloidosis; * treatment-naïve; * age ≥18 years; * ability to understand and willingness to sign an informed consent; * planned follow-up at participating center. Exclusion Criteria: * non-AL amyloidosis; * previous treatment for AL amyloidosis.
Where it's running
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Medical Department, Amyloidosis Center, University Hospital, Im Neuenheimer Feld 672
Heidelberg, Germany Recruiting -
Fondazione IRCCS Policlinico San Matteo, Pavia, Viale Golgi 19, 27100
Pavia, Italy Recruiting -
UMC Utrecht, dept Hematology, Amyloid Expertise Center, Utrecht, Heidelberglaan
Utrecht, Netherlands Recruiting -
Instituto de Investigación Sanitaria de Navarra (IdiSNA) C. de Irunlarrea, 3, 31008 Pamplona, Navarra
Pamplona, Spain Recruiting -
Universidad de la Republica Hospital de Clinicas "Dr Manuel Quintela"
Montevideo, Uruguay Recruiting -
University of Applied Sciences and Arts Northwestern Switzerland, Institute of Medical Engineering and Medical Informatics
Muttenz, Switzerland Active not recruiting
Study contacts
- Study coordinator: Giovanni Palladini
- Email: segreteria.amiloidosi@smatteo.pv.it
- Phone: +390382502994
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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SMS text check-ins to track symptoms for people with plasma cell disorders
This study tests whether daily SMS symptom prompts are feasible and acceptable for adults starting treatment for multiple myeloma or AL amyloidosis.
-
Hungarian National Systemic Amyloidosis Registry
This registry collects medical data from adults with systemic amyloidosis across Hungary to help understand how the disease is diagnosed and treated in real-world practice.
-
Tec Dara for newly diagnosed multiple myeloma with light chain amyloidosis
This study tests whether tec listamab plus daratumumab can help newly diagnosed multiple myeloma with AL amyloidosis and whether the combination is safe.
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How the IGLV1-44 light chain causes AL amyloidosis and POEMS
This project tests whether specific IGLV1-44 light‑chain sequences drive AL amyloidosis and POEMS and whether nanobodies can recognize and stabilize those light chains in adults with AL amyloidosis, POEMS, or multiple myeloma.
-
How N-glycosylation of light chains affects AL amyloidosis diagnosis and treatment
This project will test whether a sugar modification called N-glycosylation on immunoglobulin light chains helps cause disease or changes how AL amyloidosis and related monoclonal gammopathies behave in adults.
-
Belgian Amyloidosis Biobank and Patient Registry at UZ Leuven
This project collects and stores blood, tissue samples, and medical data from adults with suspected or confirmed amyloidosis to create a biobank and registry for future research.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.