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Wellbeing Digital Sciences’ Subsidiary KGK Science Forms Tactical Partnership with Nova Mentis

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The Companies Plan to Jointly Submit a Psilocybin Clinical Trial Application to Health Canada

VANCOUVER, British Columbia, Jan. 27, 2022 (GLOBE NEWSWIRE) -- KetamineOne Capital Limited (“Ketamine One” or the “Company”) (NEO: MEDI) (OTC: KONEF) (Frankfurt: MY0), an evidence-based healthcare company focused on innovative clinical solutions, artificial intelligence-powered digital therapeutics and contract research, is pleased to announce that its wholly owned subsidiary, KGK Science Inc., (“KGK”), has formed a tactical partnership with Nova Mentis Life Science Corp. (“Nova”) (FSE: HN3Q) (OTCQB: NMLSF) to help develop Nova’s psychedelic psilocybin drug portfolio in Canada. Nova is a biotechnology company and global leader in first-in-class psilocybin-based therapeutics and complementary diagnostics for neuroinflammatory disorders. Both Companies plan to jointly submit a clinical trial application (“CTA”) to Health Canada for a Phase 2A clinical study evaluating psilocybin microdose therapy for fragile X syndrome.

“I am delighted to work with Nova’s team to advance this novel initiative. Nova’s microdose approach aims to address an unmet need that promises to have a significant impact on the lives of families impacted by Fragile X Syndrome. KGK is proud to be able to contribute and is confident our expertise will guide Nova to success through the Orphan drug pathway,” said Najla Guthrie, President and CEO of KGK.

“Nova and KGK have synergistic capabilities that will facilitate submission of the CTA to Health Canada and achieve, in my opinion, no objection to this unprecedented clinical study,” stated Marvin S. Hausman MD, Nova SAB Chairman. “In our discussions with KGK, we realized early on that our two teams had the ability to navigate the entire lifecycle journey of our novel psilocybin microdose treatment of Fragile X Syndrome from a Phase 2A clinical study to drug approval and commercialization.”

Nova’s research and clinical team initially identified unique opportunities in psychedelic drug development and chose a classic drug development pathway involving careful planning and execution of chemistry, manufacturing and preclinical proof of efficacy studies. The Company’s successes to date include but are not limited to:

  • Nova is the first biotech company to achieve psilocybin orphan drug designation in both the United States and European Union;

  • Manufactured a large supply of >98% pure psilocybin for clinical studies and commercialization after drug approval;

  • Proof of efficacy and safety in preclinical rat models of Autism Spectrum Disorder and FXS with 4 studies completed;

  • Established psilocybin microdose levels to treat FXS; and

  • Preparing Phase 2 chemistry and manufacturing file for regulatory submission.