Welcome to our dedicated page for Optimi Health news (Ticker: OPTHF), a resource for investors and traders seeking the latest updates and insights on Optimi Health stock.
Optimi Health Corp. (OPTHF) is a Health Canada-licensed manufacturer specializing in GMP-certified psychedelic substances for therapeutic research. This page provides investors and researchers with verified updates on the company’s regulatory progress, clinical partnerships, and production capabilities.
Access comprehensive coverage of Optimi Health’s developments including export agreements, compliance milestones, and research initiatives. Users will find press releases related to pharmaceutical-grade psilocybin production, MDMA formulation advancements, and international distribution partnerships across regulated markets.
Key updates focus on Health Canada licensing status, GMP manufacturing standards, clinical trial support, and strategic collaborations with global research organizations. All content is curated to meet investor needs for timely, accurate information in the evolving psychedelic pharmaceuticals sector.
Bookmark this page for streamlined access to Optimi Health’s official announcements. Check regularly for updates on regulatory approvals and advancements in psychedelic-assisted therapy research.
Optimi Health, a Health Canada licensed psychedelics pharmaceutical manufacturer, has signed a Letter of Intent (LOI) with ATMA Journey Centers to supply GMP natural psilocybin for ATMA's Phase II clinical trial targeting Major Depressive Disorder (MDD). The LOI outlines a future definitive agreement within 45 days, making Optimi the sole supplier of psilocybin drug candidates for ATMA, with shared revenue from future net sales.
Optimi will also support product development for ATMA's Phase III clinical trial in 2025. The collaboration includes territories such as Canada, the US, the UK, and the EU, aiming to provide cost-effective psilocybin-assisted therapy. This partnership is expected to generate significant clinical data and improve accessibility and affordability of psychedelic therapies.
Both companies emphasize the cost-saving benefits of group therapy protocols, which reduce clinician demand and enhance patient access. By 2024-2025, Optimi aims to complete Phase II and III trials, potentially securing breakthrough therapy status.
Optimi Health Corp announced the receipt of a Certificate of Analysis (COA) confirming that its 40mg and 60mg MDMA capsules meet Good Manufacturing Practice (GMP) specifications. The capsules have a purity level of 99.95% and have passed stability testing for up to three months. The company has also completed GMP process validation for up to 1,000 capsules per batch. In a corporate update, Optimi announced plans to close a final tranche of its private placement offering, aiming to raise CAD$1,500,000 at CAD$0.30 per unit. Proceeds will be used for obtaining a Drug Establishment License and commercialization efforts.
Optimi Health Corp., a Health Canada licensed GMP psychedelics pharmaceutical manufacturer, is closing the final tranche of its non-brokered private placement to raise up to CAD$1,500,000. The Company has already raised CAD$555,010. Each Unit consists of a Common Share and a Warrant. The net proceeds will be used to obtain a Drug Establishment License, facilitate commercialization, and for general working capital. Optimi has entered into a services agreement with Very Polite Agency Inc. to provide public and media relations services. The Company has completed its Drug Establishment License inspection for GMP compliance.
Optimi Health Corp. receives an Export Permit from Health Canada to ship MDMA to Tel Aviv University's Institute for Psychedelic Research, marking its first international export. This collaboration signifies a significant milestone for Optimi, showcasing its ability to produce GMP psychedelic pharmaceuticals and support global psychedelic research and innovation.
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