drugset / Trial / NCT06750276

A Study to Evaluate the Safety, Tolerability, PK, and PD Effects of AZD2389 in Participants With Liver Fibrosis and Compensated Cirrhosis.

NCT06750276

Phase 2 Completed 40 enrolled AstraZeneca
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to measure the safety, tolerability, and the way the body absorbs, distributes, and metabolises AZD2389 as compared to placebo in participants with liver fibrosis and compensated cirrhosis. The study will also examine how the drug acts on the body

Timeline

Start
2024-12-06
Primary completion
2025-07-28
Completion
2025-07-28

Drugs

EvaluationDrugModalityDoseRoute
Subject AZD2389 Small molecule Oral