About this trial
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.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
diagnosis of systemic AL amyloidosis;
treatment-naïve;
age ≥18 years;
ability to understand and willingness to sign an informed consent;
Disqualifiers
non-AL amyloidosis;
previous treatment for AL amyloidosis.
Trial population
400 patients with AL amyloidosis will be enrolled at diagnosis and evaluated at any of the participating clinical centers.
Trial design
Cohort
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Mortality at 24 months by stage
Mortality at 24 months by stage will be evaluated
Secondary outcomes
Rate of hematologic relapse in Complete Response patients at 2 years by MRD status
Rate of hematologic relapse in Complete Response patients at 2 years by MRD status will be evaluated
Sponsors and contacts
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