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Nova Mentis Life Science Corp C.NOVA

Alternate Symbol(s):  NMLSF

Nova Mentis Life Science Corp. is a Canadian biotechnology company. The Company is engaged in developing diagnostics and psilocybin-based therapeutics for neuroinflammatory disorders. The Company has orphan drug designation in both the United States and European Union for the use of psilocybin in the treatment of fragile X syndrome (FXS). Its focus is to diagnose and treat debilitating chronic conditions that have unmet medical needs, such as autism spectrum disorder (ASD) and FXS. Its core scientific focus is on chronic neuroinflammatory conditions, which fall under three categories: neurodevelopmental, neurometabolic, and neurodegenerative. The Company operates in one segment, being research and development of psilocybin, and in one geographic area, being Canada, through its wholly owned subsidiaries, Nova Mentis Biotech Corp., and SwabAi Diagnostics Inc.


CSE:NOVA - Post by User

Post by Traderstock101on Nov 02, 2021 1:10pm
102 Views
Post# 34078085

Nova Mentis receives FDA OK for orphan drug application $$$$

Nova Mentis receives FDA OK for orphan drug application $$$$

2021-11-02 09:04 ET - News Release

 

Mr. Will Rascan reports

U.S. FDA APPROVES NOVA MENTIS ORPHAN DRUG APPLICATION

The U.S. Food and Drug Administration has approved Nova Mentis Life Science Corp.'s proprietary psilocybin drug orphan drug application to treat patients with fragile X syndrome (FXS), the most common inherited cause of autism spectrum disorder (ASD).

"Nova has established a unique position in the field of psychedelic therapy by having its FXS program achieve orphan drug status in both the United States and European Union,"says Will Rascan, NOVA's CEO & President. "I am pleased to announce that we are the first biotech company to have psilocybin registered for treatment of FXS in the drug regulatory logs of both the FDA and EMA."

Medicines that have been granted an orphan designation from the U.S. Food and Drug Administration (FDA) and European Medicines Agency (EMA) receive benefits, including but not limited to:

Seven-Ten years of market exclusivity: FDA and EMA cannot approve the same drug for the same indication.

25% federal tax credit for expenses incurred in conducting clinical research within the United States.

Waiver of Prescription Drug User Fee Act (PDUFA) fees: a value of approximately $2.9 million.

Ability to qualify to compete for research grants from the Office of Orphan Products Development (OOPD) to support clinical studies.

Eligibility to receive regulatory assistance and guidance from the FDA in the design of an overall drug development plan.

"The attainment of Orphan Drug status in both the U.S. and Europe is a significant milestone towards launch of psilocybin FXS phase 2 clinical studies," stated Dr. Marvin S. Hausman MD, Chairman of NOVA's Scientific Advisory Board. "The U.S. FDA has issued guidance concerning the usage of observational clinical study Real-World Evidence (RWE) to support the potential benefits of a medical product (1). NOVA intends to immediately launch an IRB approved ASD observational study to provide baseline clinical biomarker RWE data in support of its psilocybin IND to treat FXS."

About Nova Mentis Life Science Corp.

Nova Mentis Life Science Corp. is a Canadian-based biotechnology company and global leader in developing diagnostics and psilocybin-based therapeutics for neuroinflammatory disorders. The goal is to diagnose and treat debilitating chronic conditions that have unmet medical needs, such as autism spectrum disorder (ASD) and Fragile X Syndrome (FXS).

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