Plain-English translation of NCT06465810 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
This study is collecting real-world information about how patients with transthyretin amyloidosis—a rare disease where abnormal proteins build up in the heart, nerves, or both—are being treated and how they fare over time. Researchers will gather this information from your regular doctor visits and medical records to better understand treatment patterns and outcomes for this condition.
Transthyretin amyloidosis is a serious but rare disease, and doctors need more information about how different patients respond to current treatments and what their long-term outcomes look like. By collecting real-world data from many patients across different countries, researchers hope to improve how this disease is diagnosed, treated, and managed.
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You would continue seeing your regular doctors and following your normal treatment plan—nothing changes about your medical care. The only additional involvement is completing short electronic surveys about your health every 6 months during your routine appointments, and allowing researchers to collect information from your medical records. The study will follow you for at least 3 years, and possibly up to 7 years depending on when you enroll.
AI-generated summary from trial data · Jun 25, 2026 · Not medical advice
United States