Study identifier:D928DC00001
ClinicalTrials.gov identifier:NCT05746559
EudraCT identifier:2022-501802-36
CTIS identifier:N/A
ARTEMIS: RAvulizumab to PRotect PaTients with Chronic Kidney DisEase (CKD) froM Cardiac Surgery Associated Acute Kidney Injury (CSA-AKI) and Subsequent Major Adverse Kidney Events (MAKE): A Phase 3, Randomized, Double-blind, Placebo-controlled, Multicenter Study
Chronic Kidney Disease, CKD
Phase 3
No
Placebo, Ravulizumab
All
736
Interventional
18 Years - 90 Years
Allocation: Randomized
Endpoint Classification: -
Intervention Model: Parallel Assignment
Masking: -
Primary Purpose: Treatment
Verified 01 Aug 2024 by Alexion Pharmaceuticals, Inc.
Alexion Pharmaceuticals, Inc.
-
No locations available
Arms | Assigned Interventions |
---|---|
Placebo Comparator: Placebo Participants will receive a single weight-based dose of placebo via intravenous infusion, 1 to 7 days prior to surgery. | Drug: Placebo Participants will receive a single weight-based dose of placebo via intravenous infusion. |
Experimental: Ravulizumab Participants will receive a single weight-based dose of ravulizumab, via intravenous infusion, 1 to 7 days prior to surgery. | Drug: Ravulizumab Participants will receive a single weight-based dose of ravulizumab via intravenous infusion. |