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Taking people in GermanyNo phase

Follows adults with heart-related transthyretin amyloidosis treated with vutrisiran

Observes adults with transthyretin amyloidosis heart disease receiving vutrisiran in routine care.

Key facts

Who runs it
Alnylam Pharmaceuticals
Where
Heidelberg, Munich, Münster, and Würzburg, GermanySee the 4 sitesAlso in 2 other countries, 23 sites
Trial code
Registry title
DemonsTTRate: A Global, Observational, Multicenter, Long-term Study of Patients With ATTR-CM in a Real-World Setting
Status
Recruiting
People taking part
2,000 people, planned
Started
9 Jan 2026
Expected to end
23 Oct 2030
Type of study
Observational
Record updated
9 October 2026

Who can take part

AI summary

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for adults with transthyretin amyloidosis with cardiomyopathy (ATTR-CM) who are starting treatment with vutrisiran or another approved ATTR-CM therapy.

Age
18 years or older
Sex
All sexes can join
Disease stage
A diagnosis of ATTR-CM (transthyretin amyloidosis with cardiomyopathy)
Earlier treatment
People are starting treatment with vutrisiran or another approved ATTR-CM therapy.

Main reasons for not taking part

  • Being enrolled in an interventional clinical trial

The registry criteria, word for word

Show all 3 criteriaShow less

Who can take part

  • Has a diagnosis of ATTR-CM
  • Is initiating treatment with vutrisiran or another approved ATTR-CM therapy

Who cannot take part

  • Is enrolled in an interventional clinical trial

Where in Germany

Also in 2 other countries, 23 sites

  • Heidelberg, Baden-WurttembergHospital not named in the registryTaking people
  • MunichHospital not named in the registryTaking people
  • MünsterHospital not named in the registryTaking people
  • WürzburgHospital not named in the registryTaking people

About the trial

What the trial wants to find out

The purpose of this study is to:

Read full original descriptionShow less

* 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

The group in the trial

  • Patients with ATTR-CM

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Data and sources

Registry record
Listed on ClinicalTrials.gov.
Official title
DemonsTTRate: A Global, Observational, Multicenter, Long-term Study of Patients With Transthyretin-Mediated Amyloidosis With Cardiomyopathy in a Real-World Setting
Plain-language title
Follows adults with heart-related transthyretin amyloidosis treated with vutrisiranGenerated from the registry record. The registry title is the official one.
AI summary
From the trial's eligibility criteria. Read by machine on 13 November 2026.
Record updated
9 October 2026