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MediciNova's MN-001 successful in mid-stage NASH study

Published 04/02/2018, 07:08 AM
© Reuters.  MediciNova's MN-001 successful in mid-stage NASH study
MNOV
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  • Aimed at accelerating development, MediciNova (NASDAQ:MNOV) announces the early termination of its proof-of-principle, open-label Phase 2 clinical trial of MN-001 (tipelukast) in patients with nonalcoholic steatohepatitis (NASH) or nonalcoholic fatty liver disease (NAFLD) with excessive levels of triglycerides in their blood (hypertriglyceridemia).
  • An interim analysis showed that the study met the co-primary endpoint of a statistically significant reduction in mean serum triglycerides after eight weeks of treatment.
  • On the safety front, no clinically significant safety signals were observed.
  • Detailed results will be presented at the International Liver Congress 2018 on Friday, April 13, in Paris.
  • Tipelukast is a small molecule anti-fibrotic and anti-inflammatory compound that exerts its effects via several mechanisms, including leukotriene receptor antagonism and inhibiting enzymes known as phosphodiesterases as well as 5-lipoxygenase. It is also under development for the treatment of moderate-to-severe ideopathic pulmonary fibrosis.
  • Previously: MediciNova initiates mid-stage study of MN-001 for elevated triglycerides in NASH patients (Nov. 19, 2015)
  • Now read: Your Daily Pharma Scoop: Heron Offering, Sorrento Issues Letter To Shareholders, MediciNova Setback


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