drugset / Trial / NCT06054815

Study to Evaluate the Efficacy and Safety of DA-1241 in Subjects With Presumed NASH

NCT06054815

Phase 2 Completed 109 enrolled NeuroBo Pharmaceuticals Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

A multicenter, randomized, double-blind, placebo-controlled, parallel, Phase 2a clinical trial to evaluate the efficacy and safety of DA 1241 in subjects with presumed non-alcoholic steatohepatitis (NASH).

Timeline

Start
2023-09-14
Primary completion
2024-10-24
Completion
2024-10-30

Drugs

EvaluationDrugModalityDoseRoute
Subject DA-1241 Unknown Oral
Subject Sitagliptin Small molecule Oral