Actively Recruiting

Age: 18Years +
All Genders
NCT07358078

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

Led by Alnylam Pharmaceuticals · Updated on 2026-04-24

2000

Participants Needed

4

Research Sites

249 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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

CONDITIONS

Official Title

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

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Has a diagnosis of ATTR-CM
  • Is initiating treatment with vutrisiran or another approved ATTR-CM therapy
Not Eligible

You will not qualify if you...

  • Is enrolled in an interventional clinical trial

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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+1

Trial Site Locations

Total: 4 locations

1

Clinical Trial Site

Naples, Florida, United States, 34102

Actively Recruiting

2

Clinical Trial Site

Boston, Massachusetts, United States, 02215

Actively Recruiting

3

Clinical Trial Site

New Brunswick, New Jersey, United States, 08901

Actively Recruiting

4

Clinical Trial Site

Memphis, Tennessee, United States, 38120

Actively Recruiting

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Research Team

C

Clinical Trial Information Line

CONTACT

C

Clinical Trial Information Line

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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