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Massive european effort to crack the code of rare amyloidosis

NCT ID NCT06205953

First seen Apr 18, 2026 · Last updated May 24, 2026 · Updated 12 times

Summary

This study is creating a large European registry of 400 newly diagnosed AL amyloidosis patients. Researchers will collect blood and tissue samples to study the disease at a molecular level, aiming to improve diagnosis and predict outcomes. The goal is to better understand the disease, not to test a new treatment.

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This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

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Contacts and locations

Study contacts

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

Locations

  • Fondazione IRCCS Policlinico San Matteo, Pavia, Viale Golgi 19, 27100

    RECRUITING

    Pavia, Italy

    Contact

    Contact

    Contact

  • Instituto de Investigación Sanitaria de Navarra (IdiSNA) C. de Irunlarrea, 3, 31008 Pamplona, Navarra

    RECRUITING

    Pamplona, Spain

    Contact

    Contact

  • Medical Department, Amyloidosis Center, University Hospital, Im Neuenheimer Feld 672

    RECRUITING

    Heidelberg, Germany

    Contact

    Contact

    Contact

  • UMC Utrecht, dept Hematology, Amyloid Expertise Center, Utrecht, Heidelberglaan

    RECRUITING

    Utrecht, Netherlands

    Contact

    Contact

  • Universidad de la Republica Hospital de Clinicas "Dr Manuel Quintela"

    RECRUITING

    Montevideo, Uruguay

    Contact Phone: •••-•••-•••• Email: •••••@•••••

    Contact

  • University of Applied Sciences and Arts Northwestern Switzerland, Institute of Medical Engineering and Medical Informatics

    ACTIVE_NOT_RECRUITING

    Muttenz, Switzerland

Conditions

Explore the condition pages connected to this study.