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NCT07358078Recruiting

DemonsTTRate: A Global, Observational, Multicenter, Long-term Study of Patients With ATTR-CM in a Real-World Setting

Alnylam Pharmaceuticals

Start Date

1/9/2026

Completion Date

10/23/2030

Summary

The purpose of this study is to: * Describe the clinical characteristics of adult patients with transthyretin-mediated amyloidosis with cardiomyopathy (ATTR-CM) treated with vutrisiran in routine clinical care * Describe treatment patterns of adult patients with ATTR-CM treated with vutrisiran in routine clinical care * Assess health-related quality of life (HRQOL) in adult patients with ATTR-CM treated with vutrisiran in routine clinical care * Assess healthcare resource use (HCRU) in adult patients with ATTR-CM treated with vutrisiran in routine clinical care Compare the long-term effectiveness of vutrisiran versus other approved ATTR-CM treatments in routine clinical care

Detailed Description

Each site will invite all eligible patients to participate. Patients will be followed for up to 5 years or until patient withdrawal of consent, loss to follow-up, death, or the end of the study, whichever comes first.

Eligibility Criteria

Age Range: 18 years to No maximum

Inclusion Criteria: * Has a diagnosis of ATTR-CM * Is initiating treatment with vutrisiran or another approved ATTR-CM therapy Exclusion Criteria: * Is enrolled in an interventional clinical trial

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Conditions

Transthyretin Amyloidosis With Cardiomyopathy

Locations

Clinical Trial Site

Naples, Florida 34102

United States

Clinical Trial Site

Boston, Massachusetts 02215

United States

Clinical Trial Site

New Brunswick, New Jersey 08901

United States

Clinical Trial Site

Memphis, Tennessee 38120

United States