drugset / Trial / NCT05746559

ARTEMIS: Ravulizumab to Protect Patients With CKD From CSA-AKI and MAKE

NCT05746559

Phase 3 Completed 544 enrolled Alexion Pharmaceuticals, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary objective of this study is to assess the efficacy of a single dose of ravulizumab IV compared with placebo in reducing the risk of the clinical consequences of AKI (MAKE) at 90 days in adult participants with CKD who undergo non-emergent cardiac surgery with CPB.

Timeline

Start
2023-04-06
Primary completion
2025-10-07
Completion
2026-05-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Ravulizumab Monoclonal antibody Intravenous