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Hemostemix Announces Corporate Update

Calgary, Alberta, May 21, 2020– Hemostemix Inc. (“Hemostemix” or the “Company”) (TSXV:HEM; OTC: HMTXF) is pleased to announce that the Circuit Court of the Ninth Judicial Circuit, in and for Orange County Florida, ordered the case brought by Aspire Health Science, LLC, be reassigned to the Business Litigation Court and ordered that all pending motions be brought into compliance within 20 days. Hemostemix believes the claims are without merit and it will defend its legal positions.  A hearing is scheduled for June 29, 2020. 


Hemostemix is a publicly traded autologous stem cell therapy company. A winner of the World Economic Forum Technology Pioneer Award, the Company developed and is commercializing its lead product ACP-01 for the treatment of CLI, PAD, Angina, Ischemic Cardiomyopathy, Dilated Cardiomyopathy and other conditions of ischemia. ACP-01 has been used to treat over 300 patients, and it is the subject of a randomized, placebo-controlled, double blind trial of its safety and efficacy in patients with advanced critical limb ischemia who have exhausted all other options to save their limb from amputation.

On October 21, 2019, the Company announced the results from its Phase II CLI trial abstract entitled “Autologous Stem Cell Treatment for CLI Patients with No Revascularization Options: An Update of the Hemostemix ACP-01 Trial With 4.5 Year Followup” which noted healing of ulcers and resolution of ischemic rest pain occurred in 83% of patients, with outcomes maintained for up to 4.5 years. 

The Company owns 91 patents across five patent families titled: Regulating Stem Cells, In Vitro Techniques for use with Stem Cells, Production from Blood of Cells of Neural Lineage, and Automated Cell Therapy. For more information, please visit          

Contact: Thomas Smeenk, President, CEO & Co-Founder   905-580-4170

Neither the TSX Venture Exchange nor its Regulation Service Provider (as that term is defined under the policies of the TSX Venture Exchange) accepts responsibility for the adequacy or accuracy of this release.

Forward-Looking Information: This news release contains “forward-looking information” within the meaning ‎of applicable Canadian securities legislation. All statements, other than statements of historical fact, included ‎herein are forward-looking information. In particular, this news release contains forward-looking information ‎in relation to: the date for the first hearing and the commercialization of ACP-01‎. This forward-looking information reflects Hemostemix’s current beliefs and is based on ‎information currently available to Hemostemix and on assumptions Hemostemix believes are reasonable. ‎These assumptions include, but are not limited to: no further applications or motions delaying the date of the first hearing; no delays in the first hearing due to the COVID-19 pandemic or other reasons which require the Complex Business Litigation Court to delay the hearing; the results of ACP-01 research, trials and studies being equivalent to or better than previous research, trials or studies as well as management’s expectations of anticipated results; general and administrative costs remaining constant; the receipt of all required regulatory approvals for research, trials or studies as well as any required or desired financings of Hemostemix‎, including TSX Venture Exchange acceptance and any third party consents; the level of activity, market acceptance and market trends in the healthcare sector; the ‎economy generally; consumer interest in Hemostemix’s services and products; competition and ‎Hemostemix’s competitive advantages; and obtaining satisfactory financing to fund Hemostemix’s operations including any research, trials or studies. Forward looking information is subject to known and unknown risks, uncertainties ‎and other factors that may cause the actual results, level of activity, performance or achievements of ‎Hemostemix to be materially different from those expressed or implied by such forward-looking information. ‎Such risks and other factors may include, but are not limited to: the ability to complete its current CLI clinical trial, complete a satisfactory futility analysis and the results of such and future clinical trials; general business, economic, competitive, ‎political and social uncertainties; general capital market conditions and market prices for securities; delay or ‎failure to receive board or regulatory approvals; the actual results of future operations including the actual results of future research, trials or studies; competition; changes ‎in legislation affecting Hemostemix; the timing and availability of ‎external financing on acceptable terms; ‎long-term capital requirements and future developments in the Company’s markets and the markets in which it expects to compete;‎ lack of qualified, ‎skilled labour or loss of key individuals; and risks related to the COVID-19 pandemic including various recommendations, orders and measures of governmental authorities to try to limit the pandemic, including travel restrictions, border closures, non-essential business closures, service disruptions, quarantines, self-isolations, shelters-in-place and social distancing, disruptions to markets, economic activity, financing, supply chains and sales channels, and a deterioration of general economic conditions including a possible national or global recession; the impact that the COVID-19 pandemic may have on Hemostemix may include a decreased demand for the services that Hemostemix offers; and a deterioration of financial markets that could limit Hemostemix’s ability to obtain external financing. A description ‎of additional risk factors that may cause actual results to differ materially from forward-looking information ‎can be found in Hemostemix’s disclosure documents on the SEDAR website at Although ‎Hemostemix has attempted to identify important factors that could cause actual results to differ materially ‎from those contained in forward-looking information, there may be other factors that cause results not to be as ‎anticipated, estimated or intended. Readers are cautioned that the foregoing list of factors is not exhaustive. ‎Readers are further cautioned not to place undue reliance on forward-looking information as there can be no ‎assurance that the plans, intentions or expectations upon which they are placed will occur. Forward-looking ‎information contained in this news release is expressly qualified by this cautionary statement. The forward-‎looking information contained in this news release represents the expectations of Hemostemix as of the date ‎of this news release and, accordingly, is subject to change after such date. However, Hemostemix expressly ‎disclaims any intention or obligation to update or revise any forward-looking information, whether as a result ‎of new information, future events or otherwise, except as expressly required by applicable securities law.‎

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