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Phase 2a Study to Evaluate Safety and Explore Efficacy of J2H-1702 for NASH

Non-alcoholic Steatohepatitis Clinical Trial

Official title:
A Multi-center, Randomized, Double-blind, Placebo-controlled, Phase IIa Clinical Trial to Evaluate the Safety and Explore the Efficacy of J2H-1702 for Non-alcoholic Steatohepatitis

Clinical Trial Summary

The study aims to evaluate the safety of J2H-1702 compared to the placebo and explore the efficacy of J2H-1702 at Week 12 timepoint after administration compared to baseline in patients with NASH.

Clinical Trial Description

Subjects will be randomized to the study group 1 (J2H-1702 A mg), study group 2 (J2H-1702 B mg), study group 3 (J2H-1702 C mg), or control group (placebo of J2H-1702) in a 1:1:1:1 ratio and administered the investigational product (IP) for 12 weeks. After the IP administration, the safety and efficacy will be evaluated at V4, V8 and V12 (end of treatment, EOT). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06297434
Study type Interventional
Source J2H Biotech
Contact Eunji Byeon
Phone +82-10-8012-1074
Email ejb@j2hbio.com
Status Recruiting
Phase Phase 2
Start date February 15, 2023
Completion date January 1, 2025
View Details
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