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Hemostemix Closes $762,400 of The Unit Private Placement

Hemostemix Closes $762,400 of The Unit Private Placement

血液混合物關閉了 762,400 美元的單位私人配售
newsfile ·  2023/03/22 02:06

Calgary, Alberta--(Newsfile Corp. - March 21, 2023) - Hemostemix Inc. (TSXV: HEM) (OTCQB: HMTXF) (FSE: 2VF0) ("Hemostemix" or the "Company") is pleased to announce that it has closed its first tranche of its previously announced non-brokered private placement of units ("Units") for gross proceeds of $762,400 (the "Offering"). The Offering consisted of the issuance of an aggregate of 3,812,000 Units at a price of $0.20 per Unit.

阿爾伯塔省卡爾加裡-(Newsfile Corp.-2023年3月21日)-Hemostemix Inc.(TSXV:HEM)(OTCQB:HMTXF)(FSE:2VF0)(“血液病“或”公司“)欣然宣佈,已完成其先前宣佈的第一批非經紀私募單位(”單位“)總收益762,400美元(”供奉“)。此次發行包括以每單位0.20美元的價格發行總計3,812,000個單位。

Each Unit consists of one common share in the capital of the Company ("Common Share") and one common share purchase warrant ("Warrant"), with each full Warrant entitling the holder to acquire one Common Share at a price of $0.65 per Common Share for a period of 24 months from the closing of the Offering, subject to the accelerated expiry provision described below.

每個單位由一股本公司股本中的普通股組成(“普通股“)及一份普通股認購權證(”搜查令“),每份全面認股權證使持有人有權在發售結束後24個月內,按每股普通股0.65美元的價格收購一股普通股,但須受下述加速到期條款規限。

If during any 10 consecutive trading days occurring after four months and one day has elapsed following the closing date of the Offering, the average closing sales 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 ("Exchange") is greater than or equal to $0.80 per Common Share, the Company may provide notice in writing to the holders of the Warrants by issuance of a press release that the expiry date of the Warrants will be accelerated to the 30th day after the date on which the Company issues such press release.

如果在發行結束日期後四個月零一天後的任何連續10個交易日內,普通股在多倫多證券交易所創業板上的平均收盤價(或收盤價,如果在一個交易日沒有報告銷售)(“交易所“)大於或等於每股普通股0.80美元時,本公司可發出新聞稿,向認股權證持有人發出書面通知,表示認股權證的到期日將加快至本公司發出該新聞稿日期後的第30天。

In connection with the Offering, the Company paid eligible finders aggregate fees of $27,224 cash and issued 136,120 finder warrants to purchase Common Shares of the Company, at an exercise price of $0.20 per Common Share within 12 months from the closing of the Offering.

在此次發行中,公司向符合條件的發現者支付了總計27,224美元的現金費用,併發行了136,120份認股權證,以購買本公司的普通股,在發售結束後12個月內,行使價格為每股普通股0.2美元。

Proceeds from the Offering are expected to pay for the costs of restarting production of ACP-01, filing fees and finder fees payable in connection with the closing, and general working capital requirements.

此次發行的收益預計將用於支付重新開始生產ACP-01的成本、與關閉相關的應支付的申請費和查找費以及一般營運資金要求。

The Offering is subject to all necessary regulatory approvals including acceptance from the Exchange. All securities issued in connection with the Offering will be subject to a four-month hold period from the closing date under applicable Canadian securities laws, in addition to such other restrictions as may apply under applicable securities laws of jurisdictions outside Canada.

此次發行還需獲得所有必要的監管批准,包括獲得交易所的接受。根據適用的加拿大證券法,與此次發行相關發行的所有證券將受到自成交日期起四個月的持有期的限制,此外,加拿大以外司法管轄區適用的證券法可能適用的其他限制也可能適用。

For further details regarding the Company's Offering, please refer to the Company's News Releases dated March 8, 2023 and February 1, 2023. The Offering included subscribers under the investment dealer exemption. In accordance with the requirements of the investment dealer exemption, the Company confirms that there is no material fact or material change about the Company that has not been generally disclosed.

欲瞭解有關公司發售的更多詳情,請參閱公司於2023年3月8日和2023年2月1日發佈的新聞稿。此次發行包括投資交易商豁免範圍內的認購者。根據投資交易商豁免的要求,本公司確認本公司並無任何重大事實或重大變動未予一般披露。

ABOUT HEMOSTEMIX

關於Hemostemix

Hemostemix is an autologous stem cell therapy company, founded in 2003. A winner of the World Economic Forum Technology Pioneer Award, the Company has developed, patented, and is scaling a patient's blood-based stem cell therapeutics platform that includes angiogenic cell precursors, neuronal cell precursor and cardiomyocyte cell precursors. For more information, please visit .

Hemostemix是一家自體幹細胞治療公司,成立於2003年。作為世界經濟論壇技術先鋒獎的獲得者,該公司已經開發、申請了專利,並正在擴展患者的基於血液的幹細胞治療平臺,其中包括血管生成細胞前體、神經細胞前體和心肌細胞前體。欲瞭解更多資訊,請訪問。

For further information, please contact:
Thomas Smeenk, President, CEO & Co-Founder
EM: tsmeenk@hemostemix.com
PH: 905-580-4170

如需更多資訊,請聯繫:
託馬斯·斯米克,總裁,首席執行官兼聯合創始人
EM:郵箱:tsmeenk@hemstymx.com
電話: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.

多倫多證券交易所創業板交易所及其監管服務提供商(該術語由多倫多證券交易所創業板政策定義)均不對本新聞稿的充分性或準確性負責

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 financing of the Company and its lead product ACP-01 and the commercialization of ACP-01 via the sale of compassionate treatments subject to exemption from regulatory approval. ‎‎There can be no assurance that such forward-looking information will prove to be accurate. Actual results and future events could differ materially from those anticipated in such forward-looking information. 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: the underlying value of Hemostemix and its Common Shares; the successful resolution of the litigation that Hemostemix is pursuing or defending (the "Litigation"); the results of ACP-01 research, trials, studies and analyses, including the analysis being equivalent to or better than previous research, trials or studies; the receipt of all required regulatory ‎approvals for research, trials or studies; 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 Hemostemix obtaining satisfactory financing to ‎ fund Hemostemix's operations including any research, trials or studies, and any Litigation. 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 of Hemostemix to complete clinical trials, complete a satisfactory analyses and file the results of such analyses to gain regulatory approval of a phase II or phase III clinical trial of ACP-01; potential litigation Hemostemix mayface; 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 Hemostemix'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, disruptions to economic activity and ‎financings, disruptions to supply chains and sales channels, and a deterioration of general economic conditions including a ‎possible national or global recession or depression;the potential impact that the COVID-19 pandemic may have on Hemostemix which 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, it 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.

前瞻性資訊:本新聞稿包含適用於加拿大證券法的“前瞻性資訊”。本文中除有關歷史事實的陳述外,其他所有陳述均為前瞻性資訊。特別是,本新聞稿包含有關以下方面的前瞻性資訊:公司及其主導產品ACP-01的融資情況,以及通過銷售不受監管部門批准的體恤治療實現ACP-01的商業化。‎‎不能保證這些前瞻性資訊將被證明是準確的。實際結果和未來事件可能與這些前瞻性資訊中預期的大不相同。這些前瞻性資訊反映了Hemostemix公司目前的信念,並基於Hemostemix公司目前可獲得的資訊和Hemostemix公司認為合理的假設。這些假設包括但不限於:Hemostemix及其普通股的潛在價值;Hemostemix正在進行或辯護的訴訟的成功解決(The訴訟“);ACP-01研究、試驗、研究和分析的結果,包括分析結果等於或好於以前的研究、試驗或研究;研究、試驗或研究獲得所有必要的監管‎批准;醫療保健部門的活動水準、市場接受度和市場趨勢;‎經濟總體情況;消費者‎對Hemostemix服務和產品的興趣;競爭和‎Hemostemix的競爭優勢;以及Hemostemix獲得滿意的融資以資助‎Hemostemix的運營,包括任何研究、試驗或研究和任何訴訟。前瞻性資訊受已知和未知的風險、不確定性和其他因素的影響,這些風險、不確定性和其他因素可能會導致Hemostemix的實際結果、活動水準、業績或成就與此類前瞻性資訊明示或暗示的結果大不相同。此類風險和其他因素可能包括但不限於:Hemostemix完成臨床試驗、完成令人滿意的分析並提交分析結果以獲得監管機構對ACP-01第二階段或第三階段臨床試驗的批准的能力;可能面臨的訴訟;一般商業、經濟、競爭、政治和社會不確定性;證券的一般資本市場狀況和市場價格;延遲或未能獲得董事會或監管機構的批准;未來運營的實際結果,包括未來研究、試驗或研究的實際結果;競爭;影響Hemostemix的立法‎的變化;在可接受的條款下獲得外部融資的時機和可用性;Hemostemix市場的長期資本要求和未來發展;‎缺乏合格的熟練勞動力或失去關鍵人員;與新冠肺炎大流行有關的風險和‎,包括政府當局對‎試圖限制大流行的各種建議、命令和措施,包括旅行限制、邊境關閉、非必要企業關閉、服務中斷、隔離、自我隔離、就地避難所和社會距離、市場中斷、經濟活動和‎融資中斷、供應鏈和銷售渠道中斷、以及總體經濟狀況惡化(包括‎)可能出現的全國或全球衰退或蕭條;新冠肺炎大流行可能對血液學產生的潛在影響,可能包括對血液學提供的服務的需求減少;金融市場的惡化可能會限制Hemostemix獲得外部融資的能力。有關可能導致實際結果與前瞻性資訊大不相同的其他風險因素的描述,可在SEDAR網站上的Hemostemix披露檔案中找到。儘管Hemostemix試圖確定可能導致實際結果與前瞻性資訊中包含的結果大不相同的重要因素,但可能還有其他因素導致結果與預期、估計或預期的不同。提醒讀者,前面列出的因素並不是詳盡的。進一步告誡讀者不要過度依賴前瞻性資訊,因為不能保證這些資訊所依據的計劃、意圖或期望一定會發生。本新聞稿中包含的前瞻性資訊明確受本警示聲明的限制。本新聞稿中包含的前瞻性資訊代表了截至本新聞稿發佈之日對Hemostemix的期望,因此,在該日期之後可能會發生變化。然而,除非適用的證券法明確要求,否則Hemostemix明確不會因為新資訊、未來事件或其他原因而更新或修改任何前瞻性資訊,也不承擔任何義務。

NOT FOR DISTRIBUTION TO U.S. NEWSWIRE SERVICES OR FOR DISSEMINATION IN THE UNITED STATES

不得分發給美國新聞通訊社或在美國境內傳播

To view the source version of this press release, please visit

要查看本新聞稿的源版本,請訪問

譯文內容由第三人軟體翻譯。


以上內容僅用作資訊或教育之目的,不構成與富途相關的任何投資建議。富途竭力但無法保證上述全部內容的真實性、準確性和原創性。
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