Clinical Research Directory

Inclusion Criteria: * Age ≥18 years at diagnosis. * Diagnosed with ATTRv-CM or ATTRwt-CM, mixed phenotype. * Treated with tafamidis, as VYNDAMAX 61 mg (one 61-mg tafamidis capsule) orally once daily for ≥12 months or started on tafamidis 20 mg then switched to VYNDAMAX 61 mg for ≥12 months * Have had ≥1 pre- and ≥1 post-treatment neurologic assessments. Exclusion Criteria: * History of any organ transplant. * Individuals who are non-ambulatory. * Prior or current treatment with any disease-modifying therapy (investigational or approved) alone or in combination, except tafamidis, as VYNDAQEL 80 mg \[four 20-mg tafamidis meglumine capsules\] orally once daily or VYNDAMAX 61 mg \[one 61-mg tafamidis capsule\] orally once daily. * Peripheral neuropathy attributed to causes other than ATTR amyloidosis (eg, diabetes mellitus, B12 deficiency, hypothyroidism, shingles,Lyme disease, HIV infection, secondary to injury, chronic kidney disease). * Patient's data fails to pass data quality checks.