Study of AZD2389 Safety, Tolerability, and Pharmacodynamics in Adults With Steatotic Liver Disease and Advanced Fibrosis
Recruiting now · Phase 2 · Has a placebo group
Conditions studied: Liver Fibrosis, Hepatic Cirrhosis
In brief
The purpose of this study is to evaluate the safety, tolerability, and pharmacodynamic effects of AZD2389 in adult participants with steatotic liver disease (SLD) and advanced fibrosis.
Key facts
- Study ID
- NCT07610837
- Run by
- AstraZeneca
- People needed
- 104
- Starts
- 2026-05-07
- Expected to finish
- 2027-07-07
- Last updated by the study team
- 2026-07-29
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
Where it is running
- Research Site — Chandler, Arizona, United States (enrolling)
- Research Site — Tucson, Arizona, United States (enrolling)
- Research Site — Jupiter, Florida, United States (enrolling)
- Research Site — Miami, Florida, United States (enrolling)
- Research Site — Port Orange, Florida, United States (enrolling)
- Research Site — Kansas City, Missouri, United States (enrolling)
- Research Site — St Louis, Missouri, United States (enrolling)
- Research Site — Las Vegas, Nevada, United States (enrolling)
- Research Site — Morehead City, North Carolina, United States (enrolling)
- Research Site — Raleigh, North Carolina, United States (enrolling)
- Research Site — Westlake, Ohio, United States (enrolling)
- Research Site — Yukon, Oklahoma, United States (enrolling)
- Research Site — Clarksville, Tennessee, United States (enrolling)
- Research Site — Austin, Texas, United States (enrolling)
- Research Site — Denison, Texas, United States (enrolling)
- Research Site — Georgetown, Texas, United States (enrolling)
- Research Site — Houston, Texas, United States (enrolling)
- Research Site — Houston, Texas, United States (enrolling)
- Research Site — San Antonio, Texas, United States (enrolling)
- Research Site — San Antonio, Texas, United States (enrolling)
Full record on ClinicalTrials.gov
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