This article has been disseminated on behalf of Optimi Health Corp. and may include paid advertising.
Optimi Health (NASDAQ: OPTH) (CSE: OPTI) (FSE: 8BN) a commercial-stage pharmaceutical manufacturer of regulated psychedelic drug products, announced the completion of a GMP production run of its 5mg psilocybin finished drug product. The capsules use the same formulation currently prescribed to patients in Australia for treatment-resistant depression, with additional product from the production run designated for upcoming clinical research in the United States and clinical trials in Europe.
The company said all stages of manufacturing were completed in-house at its Health Canada-licensed facility, including biomass cultivation, active pharmaceutical ingredient extraction, encapsulation and packaging. Optimi said its vertically integrated platform and commercial-scale production capacity position the company to supply finished psilocybin and MDMA drug products to regulated markets internationally for both patient access programs and clinical research initiatives.
To view the full press release, visit https://ibn.fm/Rx3ky
About Optimi Health Corp.
Optimi Health Corp. (NASDAQ: OPTH) (CSE: OPTI) (FSE: 8BN0) is a commercial-stage pharmaceutical company focused on manufacturing and distributing GMP-grade psychedelic drug products for mental health therapies. As a Health Canada-licensed pharmaceutical manufacturer, Optimi produces validated MDMA and botanical psilocybin drug products at its GMP-compliant facilities in British Columbia, Canada.
Optimi supplies both active pharmaceutical ingredients and finished dosage forms to regulated clinical and therapeutic programs internationally, with products currently prescribed to patients in Australia under the country’s Authorized Prescriber Scheme and accessible in Canada through the Special Access Program.
For more information, please visit www.optimihealth.ca or optimi.net.
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