Registration filing
Logotype for Optimi Health Corp

Optimi Health (OPTI) Registration filing summary

Event summary combining transcript, slides, and related documents.

Logotype for Optimi Health Corp

Registration filing summary

25 May, 2026

Company overview and business model

  • Canadian GMP-compliant pharmaceutical manufacturer specializing in MDMA and psilocybin from botanical sources, licensed by Health Canada for controlled substances.

  • Vertically integrated with two 10,000 sq. ft. production facilities in Princeton, BC, operating under a Drug Establishment Licence (DEL) and Dealer's Licence (DL).

  • Products are available in Australia (prescription for PTSD and TRD), Canada (Special Access Program), and for clinical trials in Israel; U.S. market entry is pending regulatory changes.

  • Focus on scaling production, regulatory compliance, and expanding into new markets such as the U.S. and Israel.

  • Winding down nutraceutical business to focus on pharmaceutical-grade manufacturing.

Financial performance and metrics

  • Fiscal year ended September 30, 2025: revenue C$426,301 (US$306,097), net loss C$3,712,031 (US$2,665,349), accumulated deficit C$27,241,680 (US$20,001,233).

  • Three months ended December 31, 2025: revenue C$232,700, net loss C$1,553,975.

  • As of December 31, 2025: cash and cash equivalents C$491,750, total assets C$14,236,203, total liabilities C$9,219,190, shareholders' equity C$5,017,013.

  • Company has a history of operating losses and has not achieved profitability; future operations depend on raising additional capital.

Use of proceeds and capital allocation

  • Estimated net proceeds of US$12.2 million (or US$14.3 million if over-allotment is exercised) based on a US$6.00 per Unit offering price.

  • 28.7% for scaling production and distribution in current markets, 18.0% for preparing market entry to Israel and the U.S., 53.3% for general working capital and operating expenses.

  • Management has broad discretion over use of proceeds; additional funds may be needed for U.S. market entry beyond the next 12 months.

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