MediciNova Completes Enrollment in Phase 2 Trial of Tipelukast for NAFLD and Hypertriglyceridemia

Reuters11-04

MediciNova Completes Enrollment in Phase 2 Trial of Tipelukast for NAFLD and Hypertriglyceridemia

MediciNova Inc. announced the completion of patient enrollment in its Phase 2 clinical trial, MN-001-NATG-202, evaluating MN-001 (tipelukast) for the treatment of hypertriglyceridemia and non-alcoholic fatty liver disease (NAFLD) due to Type 2 diabetes. The multi-center, randomized, double-blind, placebo-controlled study is assessing the efficacy and safety of 500 mg/day of MN-001 compared to placebo over 24 weeks. Co-primary endpoints include changes from baseline in liver fat content, measured by controlled attenuation parameter (CAP) score, and fasting serum triglycerides at 24 weeks. Secondary endpoints include safety, tolerability, and changes in lipid profile. Top-line data from the trial are expected by the summer of 2026. Results have not yet been presented.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. MediciNova Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9567967-en) on November 04, 2025, and is solely responsible for the information contained therein.

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