DemonsTTRate: A Global, Observational, Multicenter, Long-term Study of Patients With ATTR-CM in a Real-World Setting
Recruiting now
Conditions studied: Transthyretin Amyloidosis With Cardiomyopathy
In brief
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
Key facts
- Study ID
- NCT07358078
- Run by
- Alnylam Pharmaceuticals
- People needed
- 2000
- Starts
- 2026-01-09
- Expected to finish
- 2030-10-23
- Last updated by the study team
- 2026-04-24
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Has a diagnosis of ATTR-CM
- Is initiating treatment with vutrisiran or another approved ATTR-CM therapy
You may not qualify if…
- Is enrolled in an interventional clinical trial
Where it is running
- Clinical Trial Site — Naples, Florida, United States (enrolling)
- Clinical Trial Site — Boston, Massachusetts, United States (enrolling)
- Clinical Trial Site — New Brunswick, New Jersey, United States (enrolling)
- Clinical Trial Site — Memphis, Tennessee, United States (enrolling)
Full record on ClinicalTrials.gov
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