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Clinical Trial Summary

This study will evaluate the efficacy and safety of vutrisiran 25 mg administered subcutaneously (SC) once every 3 months (q3M) compared to placebo in patients with ATTR amyloidosis with cardiomyopathy.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04153149
Study type Interventional
Source Alnylam Pharmaceuticals
Contact
Status Active, not recruiting
Phase Phase 3
Start date November 26, 2019
Completion date December 2026

See also
  Status Clinical Trial Phase
Active, not recruiting NCT03997383 - APOLLO-B: A Study to Evaluate Patisiran in Participants With Transthyretin Amyloidosis With Cardiomyopathy (ATTR Amyloidosis With Cardiomyopathy) Phase 3
Recruiting NCT06128629 - MAGNITUDE: A Phase 3 Study of NTLA-2001 in Participants With Transthyretin Amyloidosis With Cardiomyopathy (ATTR-CM) Phase 3