ALG-055009 in Non-cirrhotic Adults With MASH (HERALD)

NCT06342947 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 102

Last updated 2025-02-17

No results posted yet for this study

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.

Conditions

Interventions

DRUG

ALG-055009

Softgel Capsule

DRUG

Placebo

Softgel Capsule

Sponsors & Collaborators

  • Aligos Therapeutics

    lead INDUSTRY

Principal Investigators

  • Stephen Harrison, MD

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-04-01
Primary Completion
2024-08-19
Completion
2024-09-09
FDA Drug
Yes

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06342947 on ClinicalTrials.gov