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MediciNova Receives Notice of Allowance from United States Patent and Trademark Office for New Patent Covering MN-001 for Triglyceride Synthesis in the Liver
MediciNovaMediciNova(US:MNOV) GlobeNewswire News Room·2024-11-14 23:00

Core Viewpoint - MediciNova, Inc. has received a Notice of Allowance from the U.S. Patent and Trademark Office for a patent application related to MN-001 (Tipelukast), which covers a method to decrease triglyceride synthesis in the liver, particularly beneficial for patients with insulin resistance, pre-diabetes, or diabetes. The patent is expected to expire no earlier than May 26, 2042 [1][2]. Group 1: Patent and Methodology - The allowed patent claims cover a method to decrease triglyceride synthesis in the liver through the administration of MN-001 (Tipelukast) or its metabolites [1]. - MN-001 can be administered in various formulations and dosages, providing flexibility in treatment [1]. - The patent represents a significant advancement in developing treatments for metabolic disorders, emphasizing the company's commitment to innovative therapies [2]. Group 2: About MN-001 - MN-001 (Tipelukast) is a novel, orally bioavailable small molecule that exhibits anti-inflammatory and anti-fibrotic activity through multiple mechanisms, including leukotriene receptor antagonism and inhibition of phosphodiesterases [3]. - The compound has shown efficacy in down-regulating genes associated with fibrosis and inflammation, and it inhibits triglyceride synthesis in hepatocytes [3]. Group 3: Context of Metabolic Disorders - Non-alcoholic fatty liver disease (NAFLD) is linked to metabolic syndrome, with studies indicating that 50% of patients with metabolic syndrome also have NAFLD [4]. - NAFLD is associated with increased risks of cardiovascular disease, Type 2 Diabetes Mellitus (T2DM), chronic kidney disease, and malignancy, with dyslipidemia present in 20-80% of NAFLD cases [4]. Group 4: Company Overview - MediciNova, Inc. is a clinical-stage biopharmaceutical company with a late-stage pipeline focused on novel small molecule therapies for inflammatory, fibrotic, and neurodegenerative diseases [5]. - The company has 11 programs in clinical development, with its lead asset, MN-166 (Ibudilast), currently in Phase 3 trials for amyotrophic lateral sclerosis and degenerative cervical myelopathy [5].