MediciNova’s MN-001 for IPF Fails to Slow Lung Function Decline

Six months of treatment with MN-001 (tipelukast), MediciNova’s investigational oral therapy, failed to significantly improve lung function in adults with idiopathic pulmonary fibrosis (IPF), according to data from a small Phase 2 clinical trial. The therapy, however, was associated with some positive effects, such as a reduction in worsening IPF…

Potential IPF Oral Therapy, MN-001, Awarded Patent in China

MN-001, a potential treatment for idiopathic pulmonary fibrosis (IPF), will soon have patent protections in China. MediciNova, the company developing MN-001 (tipelukast), received a Notice of Allowance from the Chinese Patent Office, which means that the company’s application fulfills all necessary requirements. Once issued, the patent is expected to…

MediciNova Awaits Patent for 2 Potential Treatments for IPF and Other Fibrotic Diseases

MediciNova received a notice of allowance for a new patent covering MN-001 (tipelukast) and MN-002 (a major metabolite of MN-001) for the treatment of fibrosis,  broadly defined as wide-ranging fibrosis or fibrotic diseases, affecting different organs and due to different etiologies, including pulmonary fibrosis. Once issued by the U.S. Patent and…

MediciNova’s IPF Treatment MN-001 Receives US FDA Fast Track Designation

MediciNova, Inc., a biopharmaceutical company developing novel, small-molecule therapeutics for the treatment of diseases with unmet medical needs, recently announced that the US Food and Drug Administration has granted its leading product candidate for idiopathic pulmonary fibrosis (IPF) a Fast Track Designation. This follows the agency’s October 2014 decision to grant…

Promising Experimental IPF Drug Receives Orphan Status

MediciNova, Inc.’s idiopathic pulmonary fibrosis (IPF) drug candidate MN-001 (tipelukast) was recently granted orphan drug status by the US Food and Drug Administration. As a result, MediciNova will have exclusive rights to market MN-001 to treat patients with IPF, should it be approved following clinical trials. “We are very pleased…