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Clinical Trials in South Korea / NCT05519475
Recruiting Phase 2

A Precision Medicine Approach Using Gene Silencing to Treat a Chronic Liver Disease Called Metabolic Dysfunction-Associated Steatohepatitis (MASH) in Adult Participants at Increased Genetic Risk for This Condition

NCT05519475 · tracked via the Priya Life Science South Korea tracker
Phase
Phase 2
Started
2023-02-09
Last updated
2026-09-25

Condition(s) studied

Metabolic Dysfunction-Associated SteatoHepatitis (MASH)

Investigational drug(s) / intervention(s)

ALN-HSDPlacebo

ALN-HSD: Administered per the protocol

Placebo: Administered per the protocol

Study summary

This study is researching an investigational drug, ALN-HSD called "study drug". This study is focused on participants who are known to have Metabolic dysfunction-Associated SteatoHepatitis (MASH). MASH is a form of Metabolic dysfunction-Associated Steatotic Liver Disease (MASLD). MASH occurs when fat builds up in liver cells, damaging them, and making the liver inflamed and stiff from fibrosis (scar tissue). MASH can progress to cirrhosis (long term scarring) and liver failure (when the liver cannot perform its job). The aim of the study is to see the effect of the study drug on lessening liver scarring related to MASH.

The study is looking at several other research questions, including:

* How ALN-HSD works to improve liver function and lessen MASH-related inflammation in the liver
* What side effects may happen from receiving the study drug
* How much study drug and study drug metabolites (byproduct of the body breaking down the study drug) are in the blood at different times
* Better understanding of the study drug and MASH

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
Key Inclusion Criteria: 1. Adult male or female ≥18 years (or country's legal age of adulthood) 2. A diagnosis of MASH with Fibrosis (F) stage 2 or 3, according to the NASH-CRN 3. NAS score ≥3, as defined in the protocol 4. Meets genotype criteria for study enrollment, as defined in the protocol 5. Has a protocol defined FibroScan®-AST (FAST) score at screening or within approximately 12 weeks of screening Key Exclusion Criteria: 1. Evidence of other forms of known chronic liver disease, as defined in the protocol 2. Known history of alcohol or other substance abuse within the last year or at any time during screening, as defined in the protocol 3. History of Type 1 diabetes 4. Bariatric surgery within approximately 5 years prior to or planned during the study period 5. Prior exposure to any investigational drug targeting HSD17B13 or patatin-like phospholipase domain containing 3 (PNPLA3) (eg, ALN-HSD, ARO-HSD, ALN-PNP, AZD2693) Note: Other protocol-defined Inclusion/Exclusion Criteria apply

Primary outcome measure(s)

Trial sites (71)

FacilityCityRegionStatus
Arizona Liver Health Chandler Arizona Recruiting
The Institute for Liver Health II LLC DBA Arizona Clinical Trials - Flagstaff Flagstaff Arizona Terminated
The Institute for Liver Health II LLC DBA Arizona Liver Health - Peoria Peoria Arizona Recruiting
Adobe Clinical Research Tucson Arizona Recruiting
Arizona Liver Health - Tucson Tucson Arizona Recruiting
Del Sol Research Management, LLC Tucson Arizona Recruiting
San Fernando Valley Health Institute Canoga Park California Terminated
Velocity Clinical Research Chula Vista California Terminated
Southern California Research Center Coronado California Recruiting
Velocity Clinical Research Gardena California Terminated
Velocity Clinical Research - Huntington Park Huntington Park California Terminated
Om Research Llc Lancaster California Recruiting
Ark Clinical Research - Long Beach Long Beach California Completed
Ark Clinical Research, LLC Long Beach California Completed
Velocity Clinical Research - Westlake Los Angeles California Terminated
Clinnova Research Solutions Orange California Recruiting
Knowledge Research Center, St. Joseph's Medical Tower Orange California Recruiting
National Research Institute Panorama City California Terminated
California Liver Research Institute Pasadena California Recruiting
Cadena Care Inst. Poway California Terminated
Inland Empire Clinical Trials Rialto California Recruiting
Precision Research Institute - San Diego San Diego California Terminated
University of Colorado Anschutz Medical Campus Aurora Colorado Recruiting
Synergy Healthcare LLC Bradenton Florida Terminated
Evolution Clinical Trials Hialeah Gardens Florida Recruiting
Health Awareness, inc. Jupiter Florida Recruiting
Miami Clinical Research Miami Florida Terminated
International Medical Investigational Centers (IMIC) Incorporated Miami Florida Terminated
Genoma Research Group, Inc. Miami Florida Recruiting
US Associates in Research, LLC Miami Florida Terminated
Med Research of Florida, LLC Miami Florida Recruiting
Charter Research LLC - Orlando Orlando Florida Recruiting
Indiana University School of Medicine Indianapolis Indiana Recruiting
Deaconess Clinic - GI Specialty Center Newburgh Indiana Terminated
Tandem Clinical Research Metairie Louisiana Recruiting
Mercy Medical Center Baltimore Maryland Terminated
GI Associates Flowood Mississippi Recruiting
Washington University School of Medicine St Louis Missouri Recruiting
Columbia University Irving Medical Center New York New York Recruiting
Geisinger Medical Center Danville Pennsylvania Recruiting

+ 31 more sites — see the full list on the official registry below.

More Regeneron Pharmaceuticals trials in South Korea

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05519475 on ClinicalTrials.gov ↗ ← All trials in South Korea