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Clinical Trial Summary

The purpose of this study is to examine the changes in amyloid myocardial burden in a subset of the population participating in the ION682884-CS2 (NCT04136171) study, up to 150 participants, after treatment with eplontersen or placebo based on scintigraphy scans performed at Week 140 using the Perugini grade score method.


Clinical Trial Description

Participants who were randomized in Study ION-682884-CS2 (NCT04136171) and have had a baseline scintigraphy scan will be offered the opportunity to participate in this sub-study which involves optional scintigraphy scans. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06073587
Study type Observational
Source Ionis Pharmaceuticals, Inc.
Contact
Status Active, not recruiting
Phase
Start date April 4, 2023
Completion date March 2026