drugset / Trial / NCT06183931

Study of ALXN2220 Versus Placebo in Adults With ATTR-CM

NCT06183931 ↗

Phase 3 Active not recruiting 1181 enrolled Alexion Pharmaceuticals, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary objective of this study is to access the efficacy of ALXN2220 in the treatment of adult participants with ATTR-CM by evaluating the difference between the ALXN2220 and placebo groups as assessed by the total occurrences of all-cause mortality (ACM) and cardiovascular (CV) clinical events.

Timeline

Start
2024-01-11
Primary completion
2027-06-07
Completion
2027-10-05

Drugs

EvaluationDrugModalityDoseRoute
Subject ALXN2220 Unknown — Intravenous

Indications