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Recruiting NCT07358078

NCT07358078 DemonsTTRate: A Global, Observational, Multicenter, Long-term Study of Patients With ATTR-CM in a Real-World Setting

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Clinical Trial Summary
NCT ID NCT07358078
Status Recruiting
Phase —
Sponsor Alnylam Pharmaceuticals
Condition Transthyretin Amyloidosis With Cardiomyopathy
Study Type OBSERVATIONAL
Enrollment 2,000 participants
Start Date 2026-01-09
Primary Completion 2030-10-23

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 2,000 participants in total. It began in 2026-01-09 with a primary completion date of 2030-10-23.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief 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

Eligibility Criteria

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

Contact & Investigator

Central Contact

Clinical Trial Information Line

✉ clinicaltrials@alnylam.com

📞 1-877-ALNYLAM

Principal Investigator

Medical Director

STUDY DIRECTOR

Alnylam Pharmaceuticals

Frequently Asked Questions

Who can join the NCT07358078 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Transthyretin Amyloidosis With Cardiomyopathy. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07358078 currently recruiting?

Yes, NCT07358078 is actively recruiting participants. Contact the research team at clinicaltrials@alnylam.com for enrollment information.

Where is the NCT07358078 trial being conducted?

This trial is being conducted at Tucson, United States, Beverly Hills, United States, La Jolla, United States, Naples, United States and 11 additional locations.

Who is sponsoring the NCT07358078 clinical trial?

NCT07358078 is sponsored by Alnylam Pharmaceuticals. The principal investigator is Medical Director at Alnylam Pharmaceuticals. The trial plans to enroll 2,000 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology