drugset / Trial / NCT07608354

A Study to Evaluate the Efficacy and Safety of Concomitant Use of Eplontersen and ALXN2220 Compared With Eplontersen and Placebo for Adults Participants With ATTR-CM

NCT07608354 ↗

Phase 2 Active not recruiting 326 enrolled AstraZeneca
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this randomised, double-blind, placebo-controlled, multicenter study is to evaluate the efficacy and safety of concomitant use of eplontersen and ALXN2220 compared with eplontersen and placebo in adult participants with Transthyretin-mediated amyloid cardiomyopathy (ATTR-CM).

Timeline

Start
2026-06-11
Primary completion
2029-02-06
Completion
2029-02-06

Drugs

EvaluationDrugModalityDoseRoute
Subject ALXN2220 Unknown — Intravenous
Background Eplontersen Antisense oligonucleotide — Subcutaneous

Indications