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Clinical Trial Summary

This is a Phase 2a study to evaluate the safety, tolerability, efficacy, pharmacokinetics, and pharmacodynamics of oral (PO) daily (QD) doses of ALG-055009 (soft gelatin [softgel] capsule) for 12 weeks.


Clinical Trial Description

This is a double-blind, randomized, placebo-controlled Phase 2a study to evaluate the safety, tolerability, efficacy, pharmacokinetics, and pharmacodynamics of oral (PO) daily (QD) doses of ALG-055009 (soft gelatin [softgel] capsule) for 12 weeks. The study will be conducted in approximately 100 adult non-cirrhotic subjects with presumed MASH and liver fibrosis (F1-F3). The study will be conducted at up to approximately 45 sites throughout the United States of America. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06342947
Study type Interventional
Source Aligos Therapeutics
Contact Jen Rito
Phone (800) 466-6059
Email info@aligos.com
Status Recruiting
Phase Phase 2
Start date April 1, 2024
Completion date December 23, 2024

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