Ireland
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Priya Life Science Compound trial record
Compound · clinical trials

AZD4144 clinical trials

Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 2 trials in our USA, UK, Germany, France, Spain, Italy, Belgium, Denmark, Czechia, Turkey and Canada registers that name AZD4144 as an intervention. Synced 9 Nov 2026
2Current trials
1Recruiting now
1Lead sponsor
11Country registers
At a glance

AZD4144 is named as an intervention in 2 current clinical trials in our USA, UK, Germany, France, Spain, Italy, Belgium, Denmark, Czechia, Turkey and Canada registers. 1 is recruiting patients now. The most common phase is Phase 2. The lead sponsor is AstraZeneca. The most-studied condition is Sepsis. The EU clinical trials register (CTIS) separately lists 1 authorised or ongoing trial.

Patient leaflets for AZD4144

The package leaflet is the official guide for patients that comes with every medicine. These links go to the regulators that publish it.

  • UK
    United Kingdom: Search MHRA Products
    Patient information leaflets and SmPCs for UK-licensed products.
  • US
    United States: Search DailyMed
    FDA-approved labels, including patient and medication guides.

Leaflets differ between brands and countries; always read the one that comes with your own medicine. This is regulatory information, not medical advice.

Trials by status

  • Recruiting150%
  • Not yet open150%

Trials by phase

  • Phase 2150%
  • Phase 1150%
01

Clinical trials of AZD4144

2 trials
StudyPhaseStatusLead sponsorRegisters
A Study to Investigate the Efficacy, Safety, and Tolerability of AZD4144in Participants With Sepsis-associated Acute Kidney Injury.
NCT07215702 · Sepsis, Acute Kidney Injury
Phase 2 Recruiting AstraZeneca UK, USA, Germany, France, Spain, Italy, Belgium, Denmark, Czechia, Turkey, Canada
A Phase I Study to Investigate the Effect of Hepatic Impairment on the Pharmacokinetics, Safety, and Tolerability of AZD4144
NCT07783308 · Hepatic Impairment
Phase 1 Not yet open AstraZeneca USA

Registers list studies that are recruiting, about to open, active but closed to enrolment, or enrolling by invitation. The UK and USA registers cover industry-sponsored studies only. Trial titles and statuses are copied from the registry as published.

02

AZD4144 in the EU trials register (CTIS)

1 trial

Authorised or ongoing trials in the EU Clinical Trials Information System that list a product containing AZD4144. Many trials are registered in both CTIS and ClinicalTrials.gov, so these are shown separately rather than added to the count above. Trials with a site in Ireland are listed first.

StudyPhaseStatusSponsorCountries
A Phase IIa, Randomised, Double-blind, Placebo-controlled, Multicentre Study to Assess the Efficacy, Safety, and Tolerability of AZD4144 in Participants with Sepsis-associated Acute Kidney Injury (SERENIA)
2025-522232-13-00 · CTIS ↗ · Not possible to specify
Phase 2 Ongoing AstraZeneca AB Germany, France, Spain + 6 more
03

Conditions studied with AZD4144

3 conditions
04

Sponsors

lead sponsor per trial
Lead sponsorTrials
AstraZeneca2
05

By country register

RegisterTrialsRecruiting
Clinical trials in USA21
Clinical trials in UK11
Clinical trials in Germany11
Clinical trials in France11
Clinical trials in Spain11
Clinical trials in Italy11
Clinical trials in Belgium11
Clinical trials in Denmark11
Clinical trials in Czechia11
Clinical trials in Turkey11
Clinical trials in Canada11
EU register (CTIS)1—

A trial with sites in more than one country appears in each of those registers. CTIS does not publish a recruiting flag; its trials may also appear in the registers above.

06

Related compounds

07

Questions about AZD4144 trials

How many clinical trials are testing AZD4144?

2 current trials in our USA, UK, Germany, France, Spain, Italy, Belgium, Denmark, Czechia, Turkey and Canada registers name AZD4144 as a drug or biological intervention, as of the registry sync on 9 November 2026. Completed and withdrawn studies are not counted.

Are AZD4144 trials recruiting patients?

Yes. 1 of the 2 trials is recruiting: 1 with sites in USA, 1 with sites in UK, 1 with sites in Germany, 1 with sites in France, 1 with sites in Spain, 1 with sites in Italy, 1 with sites in Belgium, 1 with sites in Denmark, 1 with sites in Czechia, 1 with sites in Turkey and 1 with sites in Canada. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Who sponsors AZD4144 clinical trials?

The lead sponsor is AstraZeneca. The number in brackets is how many trials each organisation leads.

Where does this information come from?

Every trial, status, phase and sponsor on this page is copied from public ClinicalTrials.gov records by a daily sync. Nothing here describes how AZD4144 works or whether it is effective, and it is not medical advice.

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How this page is built

Everything on this page is copied from public ClinicalTrials.gov registry records — it is not written from memory, and nothing here describes how AZD4144 works or whether it is effective. Each trial links to its own record so you can check it yourself.

This page is built automatically: a daily sync job reads the registry records behind our country trial registers, collects every trial that lists AZD4144 (or a registered synonym) as a drug or biological intervention, and tabulates the registry fields directly. Placebos and generic comparators are excluded. There is no AI drafting and no per-compound editorial pass, and the page has not been clinically reviewed. The “last verified” date above is the timestamp of that sync, not a review date. Our general editorial approach is described in our editorial standards and corrections policy. The ClinicalTrials.gov data on this page was last retrieved on 9 Nov 2026. How every register is built: methodology · fixes we have made: corrections log.

Please verify before you rely on this. This page is general information for life-science and pharmaceutical professionals. It is not medical advice, and it has not been reviewed by a clinician — our editorial team holds life-science qualifications, not clinical ones. It is not exhaustive and may not reflect the most recent label change. Always check the official prescribing information (US Prescribing Information or EU SmPC) and speak to your doctor or pharmacist before acting on anything here. Drugs in the same class are not automatically interchangeable, and approvals, brand names and indications differ between the US, the EU/Ireland (EMA/HPRA) and other regions. Spotted an error? Tell us — we correct promptly and log it.