07:43:46 EDT Fri 31 Jul 2026
Enter Symbol
or Name
USA
CA



Hemostemix Inc (2)
Symbol HEM
Shares Issued 204,996,448
Close 2026-07-30 C$ 0.06
Market Cap C$ 12,299,787
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Hemostemix closes $322,250 second tranche of placement

2026-07-31 05:48 ET - News Release

Mr. Thomas Smeenk reports

HEMOSTEMIX CLOSES SECOND TRANCHE OF PRIVATE PLACEMENT AND OBTAINS EXTENSION TO AUGUST 14, 2026

Hemostemix Inc. has closed the second tranche of its previously announced non-brokered private placement of units, as originally disclosed on June 17, 2026. The company raised aggregate gross proceeds of $322,250 under the second tranche through the issuance of 6,445,000 units at a price of five cents per unit. Each unit consists of one common share in the capital of the company and one-half of one common share purchase warrant. Each whole warrant entitles the holder to acquire one additional common share at a price of 12 cents per share for a period of 24 months from the closing date of the second tranche of the offering, subject to the accelerated expiry provision described below. If, during any 10 consecutive trading days occurring after four months and one day has elapsed following the closing date of the offering, the volume-weighted average trading price of the common shares (or the closing bid, if no sales were reported on a trading day) as quoted on the TSX Venture Exchange is greater than or equal to 15 cents per common share, the company may accelerate the expiry date of the warrants to the date that is 30 days following the date on which the company issues a news release announcing the acceleration.

In connection with the second tranche of the offering, the company paid eligible finders aggregate cash finders' fees of approximately $21,780 and issued 435,600 finder warrants. Each finder warrant entitles the holder to purchase one common share at an exercise price of six cents per share for a period of 24 months from the closing date of the second tranche.

The proceeds of the offering are expected to be used for, sales, marketing, patient acquisition, physician education and commercialization initiatives; production and manufacturing expenses associated with ACP-01 treatments; regulatory and filing fees associated with submissions to the Ministry of Health and Wellness of the Commonwealth of the Bahamas; and general working capital and corporate purposes.

The offering remains subject to final acceptance by the exchange. All securities issued in connection with the second tranche of the offering are subject to a statutory hold period of four months plus one day from the closing date in accordance with applicable Canadian securities laws, in addition to such other restrictions as may apply under applicable securities laws of jurisdictions outside of Canada.

The TSX-V has granted the company an extension to Aug. 14, 2026, to close the balance of the non-brokered private placement of $1-million.

About Hemostemix Inc.

Hemostemix is an autologous stem cell therapy platform company, founded in 2003. A winner of the World Economic Forum technology pioneer award, the company has developed, has patented, is scaling and is selling autologous (patient's own) blood-based stem cell therapy, VesCell, an investigational autologous stem cell therapy developed to support circulation in areas affected by diseases of ischemia. VesCell is derived from a patient's own blood and evaluated through structured clinical research. Hemostemix has completed seven clinical studies of 318 subjects and published its results in 11 peer-reviewed publications. ACP-01 is safe, and appears clinically relevant, as a treatment for peripheral arterial disease, chronic limb threatening ischemia, non-ischemic dilated cardiomyopathy, ischemic cardiomyopathy, congestive heart failure and angina. Hemostemix completed its phase 2 clinical trial for chronic limb threatening ischemia and published its results in the Journal of Biomedical Research & Environmental Science. As compared with a five-year mortality rate of 50 per cent in the CLTI diabetes-based patient population, the University of British Columbia and the University of Toronto reported to the 41st meeting of vascular surgeons: 0 per cent mortality, cessation of pain and wound healing in 83 per cent of patients followed for up to 4.5 years, as a midpoint result.

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