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Terminated Phase 3 Interventional Results available

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

ClinicalTrials.gov ID: NCT05746559

Public ClinicalTrials.gov record NCT05746559. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 30, 2026, 6:57 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT05746559
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Alexion Pharmaceuticals, Inc.
Industry
Enrollment
555 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 90 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 6, 2023 (Actual)
Primary completion
Oct 7, 2025 (Actual)
Completion
May 7, 2026 (Actual)
Last update posted
Oct 29, 2026

2023 – 2026

United States locations

U.S. sites
16
U.S. states
11
U.S. cities
16
Facility City State ZIP Site status
Research Site Orange California 92868 —
Research Site San Francisco California 94143 —
Research Site Stanford California 94305 —
Research Site Chicago Illinois 60637 —
Research Site Boston Massachusetts 02115 —
Research Site Springfield Massachusetts 01107 —
Research Site Kansas City Missouri 64111 —
Research Site Rochester New York 14621 —
Research Site Valhalla New York 10595 —
Research Site Fargo North Dakota 58102 —
Research Site Philadelphia Pennsylvania 19140 —
Research Site Charleston South Carolina 29425 —
Research Site Dallas Texas 75390 —
Research Site Charlottesville Virginia 22908 —
Research Site Richmond Virginia 23298 —
Research Site Seattle Washington 98195 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 114 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05746559, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 29, 2026 · Synced Oct 30, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05746559 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →