drugset / Trial / NCT04816916

Efficacy and Safety of AXA1665 in Cirrhotic Subjects With Prior Overt Hepatic Encephalopathy

NCT04816916 ↗

Phase 2 Terminated 12 enrolled Axcella Health, Inc
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a global study to compare the effects of AXA1665, an orally active mixture of amino acids, compared to placebo, on cognitive and physical function, as well as the safety and tolerability of AXA1665.

Timeline

Start
2021-06-29
Primary completion
2022-06-30
Completion
2022-06-30

Outcome

Outcome not reported

Stopped: “Sponsor is stopping the study to focus company resources on other development programs.”

Drugs

EvaluationDrugModalityDoseRoute
Subject AXA1665 Other / unclassified 53.8 g —