Hemostemix Announces Engagement of Oak Hill Asset Management Inc.
Hemostemix Announces Engagement of Oak Hill Asset Management Inc.
Calgary, Alberta--(Newsfile Corp. - March 7, 2024) - Hemostemix Inc. (TSXV: HEM) (OTCQB: HMTXF) (FSE: 2VF0) ("Hemostemix" or the "Company") is pleased to announce the non-exclusive engagement of Oak Hill Asset Management Inc. ("OHAM"), an Exempt Market Dealer to provide capital markets advice related to the Company's capital markets strategy. Services include advice on the structure of equity or debt capital financing and the identification of potential future investors.
艾伯塔省卡爾加里--(Newsfile Corp.,2024年3月7日)——Hemostemix Inc.(多倫多證券交易所股票代碼:HEM)(OTCQB:HMTXF)(FSE:2VF0)(“HEMOSTEMIX” 或 “公司”)欣然宣佈,非獨家聘請豁免市場交易商橡樹山資產管理公司(“OHAM”)提供與公司相關的資本市場建議資本市場策略。服務包括有關股權或債務資本融資結構的建議以及潛在未來投資者的確定。
The Company intends to raise approximately C$6 million in low-dilution capital (the "Offering"). Proceeds will be used to re-establish production of ACP-01 for sale as an exempt compassionate treatment and to complete its phase III CLTI clinical trial.
該公司打算籌集約600萬加元的低攤薄資本( “優惠”)。所得款項將用於重建作爲豁免同情療法出售的 ACP-01 的生產,並完成其三期 CLTI 臨床試驗。
Pursuant to an engagement letter between the Company and OHAM, the Company has agreed to pay OHAM a cash fee of $12,000 plus $20,000 in common shares as a work fee. Additional fees would be paid on any financing raised by OHAM.
根據公司與OHAM之間的聘用書,公司已同意向OHAM支付12,000美元的現金費外加20,000美元的普通股作爲工作費。OHAM籌集的任何融資都將支付額外費用。
Proceeds from the Offering will allow the Company to lease ready-to-occupy cGMP production capacity in Puerto Rico in 2024 and generate revenue by the end of 2025 through 30-40 exempt compassionate treatments per month, while scaling production and progressing its clinical trial. Sales of ACP for CLTI treatments will be through clinical trial sites (to patients who do not meet inclusion criteria), through limb salvage clinics and podiatrists. To-date, seven clinical trial sites have agreed to refer patients to Hemostemix for exempt compassionate treatments; and, have agreed to process up to 226 of Hemostemix's referrals to them per month.
此次發行的收益將使公司能夠在2024年租賃波多黎各隨時可用的cGMP產能,並通過每月30-40種免除同情心治療在2025年底之前創造收入,同時擴大產量和推進臨床試驗。用於CLTI治療的ACP將通過臨床試驗場所(向不符合納入標準的患者)、肢體救助診所和足病醫生進行銷售。迄今爲止,已有七個臨床試驗地點同意將患者轉介到Hemostemix接受豁免的同情治療;並同意每月處理多達226份Hemostemix向他們轉診的病例。
Puerto Rico's Act 60 legislation enables the company to obtain 50% cash back on eligible expenses including clinical trials. Additionally, ACT 60 provides the company with a 15-year 1% profit tax structure, and a 20% tax credit for offshore expenses.
波多黎各的第60號法案立法使公司能夠從包括臨床試驗在內的符合條件的費用中獲得50%的現金返還。此外,ACT 60爲公司提供了15年的1%利得稅結構,以及20%的離岸費用稅收抵免。
The structure and price of the Offering has yet to be determined and the Company will issue a follow-up news release once details are available. The Company is confident that it can be completed on a low-dilutive basis that appropriately values the significant, near-term revenue and cash flow streams.
本次發行的結構和價格尚未確定,一旦獲得詳細信息,公司將發佈後續新聞稿。該公司相信,可以在低稀釋率的基礎上完成,適當估值可觀的短期收入和現金流。
"The 498 treatments of ACP, including the seven clinical studies published in peer reviewed journals to-date, demonstrate ACP is safe and effective in the treatment of peripheral arterial disease and three forms of heart disease," stated Thomas Smeenk, CEO. "It is remarkable that the clinical trial sites will be able to refer and see up to 226 no-option referrals. Compared to no-option and amputation, an ACP injection under exemption to save the limb makes sense," Smeenk said.
首席執行官托馬斯·斯梅恩克表示:“ACP的498種治療方法,包括迄今在同行評審期刊上發表的七項臨床研究,表明ACP在治療外周動脈疾病和三種形式的心臟病方面是安全有效的。”“值得注意的是,臨床試驗場所將能夠轉診和查看多達226例無選擇轉診病例。與無選擇和截肢相比,在豁免條件下注射ACP以挽救肢體是合理的,” 斯梅恩克說。
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 是一家自體幹細胞療法公司,成立於 2003 年。作爲世界經濟論壇技術先鋒獎的獲得者,該公司開發了包括血管生成細胞前體、神經元細胞前體和心肌細胞前體在內的患者血液基幹細胞治療平台,並正在擴大其專利。欲了解更多信息,請訪問 。
For further information, please contact: Thomas Smeenk, President, CEO & Co-Founder
EM: tsmeenk@hemostemix.com PH: 905-580-4170
欲了解更多信息,請聯繫: Thomas Smeenk,總裁、首席執行官兼聯合創始人
EM: tsmeenk@hemostemix.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.
多倫多證券交易所風險交易所及其監管服務提供商(該術語由多倫多證券交易所風險交易所的政策定義)均不對本新聞稿的充分性或準確性承擔責任。
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 engagement of Oak Hill Financial, the sales of ACP-01 as an exempt compassionate treatment, the licensing of ACP-01, the Trademark Know Your Health! and related results, including the commercialization of ACP-01. 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 Hemostemis 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.
前瞻性信息:本新聞稿包含適用的加拿大證券立法所指的 “前瞻性信息”。除歷史事實陳述外,此處包含的所有陳述均爲前瞻性信息。特別是,本新聞稿包含與以下內容有關的前瞻性信息:橡樹山金融的參與、作爲豁免同情待遇的 ACP-01 的銷售、ACP-01 的許可、Know Your Health 商標!及相關成果,包括 ACP-01 的商業化。There 無法保證此類前瞻性信息會被證明是準確的。實際結果和未來事件可能與此類前瞻性信息中的預期存在重大差異。這些前瞻性信息反映了Hemostemix當前的信念,基於Hemostemix目前獲得的信息以及Hemostemix認爲合理的假設。這些假設包括但不限於:Hemostemix及其普通股的基本價值;Hemostemix提起或辯護的訴訟的成功解決(”訴訟“);ACP-01 研究、試驗、研究和分析的結果,包括分析等同於或優於先前的研究、試驗或研究;研究、試驗或研究所需的所有監管approvals 的收據;醫療保健行業的活動水平、市場接受度和市場趨勢;一般economy;Hemostemix 中的消費者interest服務和產品;競爭和Hemostemix 的競爭優勢;以及Hemostemix獲得令人滿意的融資, 爲Hemostemix的業務(包括任何研究、試驗或研究以及任何訴訟)提供資金。前瞻性信息受已知和未知風險、不確定性和其他因素的影響,這些因素可能導致Hemostemix的實際結果、活動水平、業績或成就與此類前瞻性信息所表達或暗示的結果存在重大差異。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此類分析結果以獲得監管部門批准 ACP-01 的二期或三期臨床試驗的能力;Hemostemis可能面臨的潛在訴訟;一般業務、經濟、競爭、政治和社會的不確定性;一般資本市場狀況和證券市場價格;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;立法變化affecting Hemostemix;在可接受條件下外部融資的時機和可用性;Hemostemix市場及其預期競爭市場的長期資本要求和未來發展; 缺乏合格熟練勞動力或關鍵人員流失;以及風險related 到 COVID-19 疫情,包括政府當局向try 提出的限制疫情的各種建議、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、就地避難和保持社交距離、市場中斷、經濟活動中斷以及financings,供應鏈和銷售渠道中斷,總體經濟狀況惡化,包括possible 全國或全球衰退或蕭條;COVID-19 疫情可能對Hemostemix產生的潛在影響,其中可能包括對Hemostemix提供的服務的需求減少;以及金融市場的惡化可能限制Hemostemix獲得外部融資的能力。有關可能導致實際業績與前瞻性信息存在重大差異的其他風險因素的描述,可在SEDAR網站上Hemostemix的披露文件中找到,網址爲。儘管Hemostemix試圖確定可能導致實際結果與前瞻性信息中包含的結果存在重大差異的重要因素,但可能還有其他因素導致結果與預期、估計或預期的結果不符。請讀者注意,上述因素清單並不詳盡。還提醒讀者不要過分依賴前瞻性信息,因爲無法保證他們所依據的計劃、意圖或期望會實現。本警示聲明明確限制了本新聞稿中包含的前瞻性信息。本新聞稿中包含的前瞻性信息代表了Hemostemix截至本新聞發佈之日的預期,因此,在此日期之後可能會發生變化。但是,除非適用的證券法明確要求,否則Hemostemix明確表示不打算或承擔任何更新或修改任何前瞻性信息的意圖或義務,無論這些信息是由於新信息、未來事件還是其他原因造成的。
譯文內容由第三人軟體翻譯。