ALG-055009 in Non-cirrhotic Adults With MASH (HERALD)
NCT06342947 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 102
Last updated 2025-02-17
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
-
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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