deltatrials
Recruiting OBSERVATIONAL NCT06205953

A EUropean REgistry and Sample Sharing networK to Promote the Diagnosis and Management of Light Chain Amyloidosis (EUREKA) (EUREKA)

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)

Sponsor: Fondazione IRCCS Policlinico San Matteo di Pavia

Conditions AL Amyloidosis
Updated 7 times since 2024 Last updated: Apr 13, 2026 Started: Jan 1, 2024 Primary completion: Jun 1, 2026 Completion: Jun 1, 2026
This information is for research purposes only and is not medical advice. Consult a healthcare provider before making any medical decision.

This observational or N/A phase trial investigates AL Amyloidosis and is currently actively recruiting participants. Fondazione IRCCS Policlinico San Matteo di Pavia leads this study, which shows 7 recorded versions since 2024 — indicating limited longitudinal coverage. The change history captured here reflects the iterative nature of clinical trial conduct.

Study Description(click to expand)

In the frame of the EUREKA Consortium, a patients' registry collecting all new cases of AL amyloidosis evaluated at referral Centers across Europe or at their satellite sites will be created, in association with a cross-border biorepository and sample sharing network for the study of both disease-causing light chains and plasma cells with advanced molecular technologies. A dedicated site will support the Consortium with big data analysis and artificial intelligence applied to health. The aims are: 1) Defining the impact of advanced molecular technologies to promote early diagnosis and guide therapeutic choices; 2) describing the natural history of the disease in a representative cohort of AL patients in the contemporary era of effective anti-plasma cell therapies; 3) investigating and refining novel advanced technologies to detect with high sensitivity residual disease-causing plasma cells/light chains in patients achieving a complete hematologic response to therapy (minimal residual disease, MRD).

In the frame of the EUREKA Consortium, a patients' registry collecting all new cases of AL amyloidosis evaluated at referral Centers across Europe or at their satellite sites will be created, in association with a cross-border biorepository and sample sharing network for the study of both disease-causing light chains and plasma cells with advanced molecular technologies. A dedicated site will support the Consortium with big data analysis and artificial intelligence applied to health. The aims are: 1) Defining the impact of advanced molecular technologies to promote early diagnosis and guide therapeutic choices; 2) describing the natural history of the disease in a representative cohort of AL patients in the contemporary era of effective anti-plasma cell therapies; 3) investigating and refining novel advanced technologies to detect with high sensitivity residual disease-causing plasma cells/light chains in patients achieving a complete hematologic response to therapy (minimal residual disease, MRD).

Status Flow

~Feb 2024 – ~May 2024 · 3 months · monthly snapshotRecruiting~May 2024 – ~Jul 2024 · 2 months · monthly snapshot~Jul 2024 – ~Aug 2024 · 31 days · monthly snapshot~Aug 2024 – ~Sep 2024 · 31 days · monthly snapshot~Sep 2024 – ~Dec 2024 · 3 months · monthly snapshotRecruiting~Dec 2024 – ~Apr 2026 · 16 months · monthly snapshotRecruitingApr 17, 2026 – present · 3 months · daily APIRecruiting

Change History

7 versions recorded
  1. Apr 17, 2026 — Present [daily]

    Recruiting

  2. Dec 2024 — Apr 2026 [monthly]

    Recruiting

  3. Sep 2024 — Dec 2024 [monthly]

    Recruiting

  4. Aug 2024 — Sep 2024 [monthly]

    Recruiting

  5. Jul 2024 — Aug 2024 [monthly]

    Recruiting

Show 2 earlier versions
  1. May 2024 — Jul 2024 [monthly]

    Recruiting

  2. Feb 2024 — May 2024 [monthly]

    Recruiting

    First recorded

Jan 2024

Trial started

Per CT.gov start date — pre-dates our first snapshot

Eligibility Summary

A prospective patients' registry collecting all new cases of AL amyloidosis evaluated at referral Centers from across Europe and a sample sharing network will be created to study mechanisms of the disease through the use of advanced molecular technologies and big data analysis tools.

Contact Information

Sponsor contact:
  • Fondazione IRCCS Policlinico San Matteo di Pavia
Data source: ClinicalTrials.gov

For direct contact, visit the study record on ClinicalTrials.gov .