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Study details
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A Study to Investigate the Efficacy, Safety, and Tolerability of AZD4144 in Participants With Sepsis-associated Acute Kidney Injury

AstraZeneca
NCT IDNCT07215702ClinicalTrials.gov data as of Apr 2026
Phase

Phase 2

Target enrollment

124

Study length

about 1.2 years

Ages

18–80

Locations

16 sites in AZ, CA, KS +9

What this study is about

This trial is testing a treatment called AZD4144 for people with sepsis who also have acute kidney injury. Participants will receive either AZD4144 or a placebo intravenously once daily for 436 days, along with safety monitoring and other assessments. The goal is to compare specific kidney function measurements between those receiving AZD4144 and those receiving the placebo.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take AZD4144
  • 2.Take Placebo

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Standard

How treatment is administered

Treatment Assignment
Randomized & Blinded

You may get a placebo/standard care, and you won't know which.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Endpoints

Primary: Area Under the Curve (AUC) of 24-hour Creatinine Clearance (CrCl).

Secondary: AUC mSOFA score, AUC: Plasma IL-18, AUC: Plasma IL-6, AUC: Serum Creatinine, AUC: Serum Cystatin C, AUC: Urine IL-18, AUC: Urine IL-6, AUC: mGFR

Body systems

Renal, Infectious