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3 clinical studies listed.

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Transthyretin (TTR) Amyloid Cardiomyopathy

Tundra lists 3 Transthyretin (TTR) Amyloid Cardiomyopathy clinical trials. Each listing includes eligibility criteria, study locations, and direct links to research sites in the Tundra directory.

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RECRUITING

NCT07196839

Determining the Association of TTR Stabilizing Therapy With Circulating TTR Amyloid Aggregates Over Time in Patients With ATTR-CM: Longitudinal Biomarker Study

The objective of this study is to determine the association of clinically prescribed, on-label, TTR stabilizing therapy (e.g. tafamidis or acoramidis) with levels of circulating transthyretin amyloid aggregates (TAAs, a surrogate for amyloid disease activity) measured serially over time in patients with transthyretin cardiac amyloidosis (ATTR-CA). To accomplish this objective, the hypothesis that TTR stabilizing therapy will be associated lower circulating TAAs over time will be tested. Completion of this study will advance the understanding of the influence of ATTR-CA treatments on circulating evidence of amyloidosis and justify the role of blood testing to monitor treatment response in patients with ATTR-CA.

Gender: All

Ages: 30 Years - 80 Years

Updated: 2026-01-07

1 state

Transthyretin (TTR) Amyloid Cardiomyopathy
ACTIVE NOT RECRUITING

NCT07062848

An Observational Study Using Artificial Intelligence (AI) Algorithms on Electrocardiography (ECG), Point-of-care Ultrasound (POCUS), and Transthoracic Echocardiophy (TTE) to Estimate the Under-diagnosis of Transthyretin Amyloid Cardiomyopathy (ATTR-CM) Across a Diverse Range of US Health Systems.

This is a multi-center, observational study with the overall objective to examine the scale of under-diagnosis for transthyretin amyloid cardiomyopathy (ATTR-CM) across a broad range of diverse health systems in the US using a fully federated deployment of an artificial intelligence (AI) toolkit of algorithms that detect ATTR-CM on electrocardiography (ECG), point-of-care ultrasound (POCUS), and transthoracic echocardiography (TTE).

Gender: All

Ages: 50 Years - 95 Years

Updated: 2025-07-14

10 states

Transthyretin (TTR) Amyloid Cardiomyopathy
ENROLLING BY INVITATION

NCT06714019

PL_GNT01_ISR_Grant 53234273

We carry out a prospective non-interventional, longitudinal, observational multicentre registry designed to improve our understanding of the epidemiology of TTR amyloidosis in our country. The main objective of the proposed study is to determine the occurrence of TTR amyloidosis and describe clinical profile of patients in the population of our country.

Gender: All

Ages: 18 Years - Any

Updated: 2024-12-03

Transthyretin Cardiomyopathy (TTR-CM)
Transthyretin (TTR) Amyloid Cardiomyopathy
Transthyretin Amyloidosis