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Asep Inc. Obtains Exclusive Worldwide License From the University of British Columbia for Ground-breaking Medical Device Coating Technology

Asep Inc. Obtains Exclusive Worldwide License From the University of British Columbia for Ground-breaking Medical Device Coating Technology

Asep Inc. 獲得不列顛哥倫比亞大學頒發的開創性醫療器械塗層技術的全球獨家許可
PR Newswire ·  2023/07/31 19:30

VANCOUVER, BC, July 31, 2023 /CNW/ - Asep Medical Holdings Inc. ("Asep Inc." or the "Company") (CSE: ASEP) (OTCQB: SEPSF) (FSE: JJ8) is pleased to announce that, as of July 21, 2023, it has completed the final milestone in its acquisition of SafeCoat Medical Inc. ("SafeCoat") and entered into an exclusive worldwide license agreement (the "Agreement") with the University of British Columbia ("UBC"), through its subsidiary SafeCoat, for the use, development and commercialization of a ground-breaking medical device coating technology (the "Technology").

溫哥華,卑詩省2023年7月31日/cnw/-Asep Medical Holdings Inc.(“ASEP Inc.“或”公司“)(CSE:ASEP)(場外交易市場:SEPSF)(法蘭克福證券交易所:JJ8)高興地宣佈,截至2023年7月21日,它已經完成了收購SafeCoat Medical Inc.的最後一個里程碑。安全塗層“)並簽訂獨家全球許可協定(”協定“)與不列顛哥倫比亞大學(“UBC),通過其子公司SafeCoat,用於使用、開發和商業化突破性的醫療器械塗層技術(技術“)。

Device-related infections are responsible for a quarter of all healthcare-associated infections and are difficult to treat with conventional antibiotics due to the adherence and growth of bacterial biofilms on the surface of the device. Catheters are an excellent example of medical instruments that can cause serious infections. According to the Center for Disease Control and Prevention (CDC), approximately 90% of serious infections caused by catheters are associated with central venous catheters (CVCs). Not only are CVC infections serious for the patient, but they are also costly for hospitals as the cost per infection is estimated to range from USD $34,508 to $56,000. This represents an annual cost for caring for these patients to be approximately USD $296 million — $2.3 billion in the US alone.1

與設備相關的感染佔所有與醫療保健相關的感染的四分之一,由於設備表面的細菌生物膜的黏附和生長,很難用常規抗生素治療。導尿管是可能導致嚴重感染的醫療器械的一個很好的例子。根據疾病控制和預防中心(CDC)的數據,大約90%由導管引起的嚴重感染與中心靜脈導管(CVCs)有關。CVC感染不僅對患者來說是嚴重的,而且對醫院來說也是昂貴的,因為每次感染的成本估計從34,508美元56,000美元。這意味著每年護理這些患者的成本約為美元。2.96億美元-僅在美國就有23億美元。1

The Technology encompasses two critical aspects to prevent device-related infections, which cause an additional cost of $57,0002 per patient and require replacement of the infected device. The coating includes an antimicrobial peptide conjugated to the surface of the device to kill bacteria and anti-fouling self-assembling polymers that prevent the dead bacteria from binding to the device surface and masking the killing effect. This coating technology can be applied to various surfaces, including glass, plastic and titanium, on surgical implants, catheters, pacemakers, stents, artificial limbs and organs, and contact lenses. Feasibility has been demonstrated in animal models. Device-related infections are responsible for a quarter of all healthcare-associated infections2.

該技術包括兩個關鍵方面,以防止與設備相關的感染,這會導致額外的成本57,000美元2.並且需要更換受感染的設備。該塗層包括連接到設備表面以殺滅細菌的抗菌肽,以及防止死亡細菌結合到設備表面並掩蓋殺菌效果的防汙染自組裝聚合物。這種塗層技術可以應用於外科植入物、導管、起搏器、支架、假肢和器官以及隱形眼鏡上的各種表面,包括玻璃、塑料和鈦。動物模型已經證明瞭這種方法的可行性。與設備相關的感染佔所有與醫療保健相關的感染的四分之一2.

According to Research and Markets Medical Device Coatings: Global Markets report, the estimated value of medical device coatings in 2022 was USD $5.8 billion and is estimated to grow to USD $9.7 billion by 2027, representing a compound annual growth rate (CAGR) of 10.9%3. The report also provides compelling reasons for the market's growth:

根據研究和市場醫療器械塗料:全球市場報告稱,2022年醫療器械塗層的估計價值為美元58億美元預計將增長到美元97億美元到2027年,復合年增長率(CAGR)為10.9%3.。該報告還為市場的增長提供了令人信服的理由:

  • An ageing population is driving an increased demand for medical devices
  • Advancements in technology have led to the development of new medical devices that require coatings
  • The rising incidence of chronic diseases, such as heart disease and diabetes, is driving demand for medical devices that can be used for long-term treatment
  • Along with scientific and technological advances, the FDA and other regulatory bodies have developed strict requirements to increase patient safety by improving the safety and performance of medical devices, which has led to an increased demand for coatings that can meet those requirements
  • Medical device coatings can be cost-effective in the long run by prolonging the life of the device or by reducing the need for frequent replacement4
  • 人口老齡化正在推動對醫療器械的需求增加
  • 技術的進步導致了需要塗層的新醫療器械的開發
  • 心臟病和糖尿病等慢性病發病率的上升推動了對可用於長期治療的醫療設備的需求
  • 隨著科學技術的進步,FDA和其他監管機構制定了嚴格的要求,通過改善醫療器械的安全性和性能來提高患者的安全性,這導致了對能夠滿足這些要求的塗料的需求增加
  • 從長遠來看,醫療器械塗層可以通過延長設備的壽命或減少頻繁更換的需要來實現成本效益4.

"We are excited to take this promising new technology forward through SafeCoat Medical and the exclusive worldwide license from UBC. We anticipate that this transaction will create significant new market opportunities as we tackle the problem of maintaining sterile surfaces on medical devices and implants," stated Tim Murphy, Asep Inc.'s Chief Operating Officer.

我們很高興通過SafeCoat Medical和UBC的獨家全球許可來推動這項前景光明的新技術的發展。我們預計,隨著我們解決醫療器械和植入物的無菌表面維護問題,這筆交易將創造重要的新市場機會。蒂姆·墨菲、Asep Inc.首席運營官S。

Pursuant to the Agreement, Asep Inc. will hold 88% of the issued and outstanding shares of SafeCoat. UBC and the non-waiving inventors of the Technology will collectively own the remaining 12% of the issued and outstanding shares of SafeCoat in consideration for the exclusive license grant. Dr. Robert E. W. Hancock, Founder and CEO of Asep Inc., is one of the four non-waiving inventors of the SafeCoat Technology.

根據協定,ASEP公司將持有SafeCoat公司88%的已發行和流通股。作為授予獨家許可的代價,UBC和該技術的非放棄發明者將共同擁有SafeCoat剩餘12%的已發行和流通股。Dr。羅伯特·W·漢考克,Asep Inc.的創始人兼首席執行官,是SafeCoat技術的四位不放棄發明者之一。

The term of the Agreement will expire on the later of 20 years from the grant of the license and the expiry date of the last of the patents relating to the Technology. In consideration for the granting of the license, SafeCoat will pay a royalty to UBC on the revenue generated from the commercialization of the Technology products by SafeCoat at a rate of 3.75% and at staged higher rates on sub-licenses as particularly set out in the Agreement. SafeCoat will also pay annual fees to UBC on January 1st of each year as follows: $5,000 from 2024 to 2026, $10,000 from 2027 to 2029, $15,000 from 2030 to 2032, $50,000 from 2033 and each successive year thereafter. SafeCoat will also make a milestone payment of $150,000 to UBC upon each product derived from the Technology receiving 510(k) clearance or PMA (or equivalent if outside the U.S.) approval. Certain patent management fees are also payable by SafeCoat to UBC.

本協定的有效期將在授予許可證和與該技術有關的最後一項專利的到期日起20年後到期。作為授予許可的代價,SafeCoat將向UBC支付從SafeCoat將技術產品商業化所產生的收入的特許權使用費,費率為3.75%,並按照協定中特別規定的分許可階段性更高的費率支付。SafeCoat還將於****年向UBC支付年費1月1日每一年的數目如下:5,000美元從2024年到2026年,1萬美元從2027年到2029年,15,000美元從2030年到2032年,5萬美元自2033年起及其後每一年。SafeCoat還將進行里程碑式的付款150,000美元根據技術獲得510(K)許可或PMA(如果在美國以外,則為同等產品)的每個產品提交UBC批准。SafeCoat還需要向UBC支付某些專利管理費。

Dr. Hancock, the CEO and a director of the Company is a party to the License Agreement as he is one of the non-waiving inventors; as such, the portion of the transaction with Dr. Hancock is considered to be a "related party" within the meaning of Multilateral Instrument 61-101 Protection of Minority Security Holders in Special Transactions ("MI 61-101") and the proposed issuance to Dr. Hancock of common shares of SafeCoat Medical Inc., a subsidiary of the Company, is considered to be a "related party transaction" within the meaning of MI 61-101. These related party transactions are exempt from the valuation requirement of MI 61-101 by virtue of the exemption contained in section 5.5(b) as the Company's shares are not listed on a specified market and from the minority shareholder approval requirements of MI 61-101 by virtue of the exemption contained in section 5.7(a) of MI 61-101 in that the fair market value of the consideration of the shares to be issued to each related party does not exceed 25% of the Company's market capitalization.

本公司首席執行官兼董事成員漢考克博士是許可協定的訂約方,因為他是非放棄發明人之一;因此,與漢考克博士的交易部分被視為多邊文書61-101《在特殊交易中保護少數股權持有人》所指的“關聯方”(“米其林61-101),而擬向Hancock博士發行本公司子公司SafeCoat Medical Inc.的普通股,被認為是MI 61-101所指的“關聯方交易”。該等關聯方交易因第5.5(B)節所載豁免而獲豁免遵守MI 61-101的估值規定,而由於本公司的股份並非於指定市場上市而獲豁免遵守MI 61-101的小股東批准規定,以及憑藉MI 61-101第5.7(A)節所載的豁免而獲豁免遵守MI 61-101的小股東批准規定,即將向各關聯方發行的股份代價的公平市價不超過本公司市值的25%。

ABOUT ASEP MEDICAL HOLDINGS INC.

Asep醫療控股公司簡介

Asep Medical Holdings Inc. () is dedicated to addressing the global issue of antibiotic failure by developing novel solutions for significant unmet medical needs in human medicine. The Company is a consolidation of three existing private companies, all with technology in advanced development — Sepset Biosciences Inc. (proprietary diagnostic tools to enable the early and timely identification of sepsis), ABT Innovations Inc. (broad-spectrum therapeutic agents to address multi-drug resistant biofilm infections), and SafeCoat Medical Inc. (an antibacterial peptide medical device coating technology).

Asep Medical Holdings Inc.()致力於通過為人類醫學中未得到滿足的重大醫療需求開發新的解決方案來解決抗生素失效的全球問題。該公司是由三家現有的私營公司合併而成的,它們的技術都處於高級開發階段--Sepset Biosciences Inc.(能夠及早及時識別膿毒症的專有診斷工具)、ABT Innovation Inc.(用於解決多重耐藥生物膜感染的廣譜治療劑)和SafeCoat Medical Inc.(一種抗菌肽醫療設備塗層技術)。

Sepset Biosciences Inc. () is in the final stages of preparation for clinical studies and commercialization of an in vitro diagnostic test that involves a patient gene expression signature that helps assess the development of severe sepsis, one of the significant diseases leading to antibiotic failure since antibiotics are the primary initial treatment for sepsis. Sepsis was responsible for nearly 20% of all deaths on the planet in 2017 and essentially all deaths due to COVID-19 and other pandemics. The SepsetER test is a blood-based gene expression assay that is straightforward to implement, and results are obtained about an hour after taking a blood sample in the emergency room or intensive care unit. This proprietary diagnostic technology differs from current diagnostic tests, enabling the risk assessment for progression to severe sepsis within ~60 minutes of initiating the test. Bacterial culture, the gold standard, provides results after ~15 hours but can be as long as three days. Asep Inc. believes its test will enable critical early decisions to be made by physicians regarding appropriate therapies and thus reduce overall morbidity and mortality due to sepsis.

賽普塞特生物科學公司。()正處於臨床研究和體外診斷測試商業化的最後階段,該測試涉及患者基因表達簽名,有助於評估嚴重膿毒症的發展,這是導致抗生素失效的重大疾病之一,因為抗生素是膿毒症的主要初始治療方法。2017年,膿毒症佔全球死亡人數的近20%,幾乎所有死於新冠肺炎和其他流行病的人都死於敗血癥。SepsetER測試是一種基於血液的基因表達測試,操作簡單,在急診室或重症監護病房採集血液樣本約一小時後即可獲得結果。這項專利診斷技術不同於目前的診斷測試,可以在啟動測試後約60分鐘內對進展為嚴重膿毒症的風險進行評估。細菌培養是金標準,大約15小時後就會產生結果,但可能長達3天。ASEP公司相信,它的測試將使醫生能夠就適當的治療做出關鍵的早期決定,從而降低因膿毒症而導致的總體發病率和死亡率。

ABT Innovations Inc.'s () peptide technology covers a broad range of therapeutic applications, including bacterial biofilm infections (dental, wound, sinusitis, skin, medical device infections, chronic infections, lung, bladder, ear-nose and throat, orthopaedic, etc.), anti-inflammatories, anti-infective immune-modulators and vaccine adjuvants. The company is in the pre-clinical development phase with promising data for the first three indications.

ABT創新公司的S()多肽技術涵蓋廣泛的治療應用,包括細菌生物被膜感染(牙科、傷口、鼻竇炎、皮膚、醫療器械感染、慢性感染、肺、膀胱、耳鼻喉科、骨科等)、抗炎藥物、抗感染免疫調節劑和疫苗佐劑。該公司正處於臨床前開發階段,前三個適應症的數據前景看好。

SafeCoat Medical Inc.'s () technology encompasses anti-fouling self-assembling polymers combined with conjugated antimicrobial peptides, which can be applied to various surfaces as antimicrobial and anti-fouling coatings. In particular, the invention relates to coatings that may be applied to multiple medical devices and implants, and feasibility has been demonstrated in animal models. The company's expertise also encompasses the methods for manufacturing and applying these anti-bacterial coatings.

SafeCoat醫療公司的S()技術包括防汙自組裝聚合物和結合在一起的抗菌肽,這些抗菌肽可以作為抗菌和防汙塗層應用於各種表面。具體地,本發明涉及可應用於多種醫療設備和植入物的塗層,並且已經在動物模型中證明瞭可行性。該公司的專業知識還包括製造和應用這些抗菌塗料的方法。

FORWARD-LOOKING STATEMENTS —
This news release contains certain "forward-looking statements" within the meaning of such statements under applicable securities law. Forward-looking statements are frequently characterized by words such as "anticipates," "plan," "continue," "expect," "project," "intend," "believe," "anticipate," "estimate," "may," "will," "potential," "proposed," "positioned" and other similar words, or statements that certain events or conditions "may" or "will" occur. These statements include but are not limited to the successful clinical testing of our Sepsis in vitro diagnostic test and its intended filing for regulatory market authorization; the Company not receiving regulatory market authorization as planned or at all; the undertaking of pre-clinical studies on our lead therapeutic, with the expectation that this will lead to fast-track clinical trials; the timeframe for identification of sepsis with the company's products; the potential opportunities for the generation of revenue; the therapeutic benefits of the company's products; and other statements regarding the company's proposed business plans. Various assumptions were used in drawing conclusions or making the predictions contained in the forward-looking statements throughout this news release. Forward-looking statements are based on the opinions and estimates of management at the date the statements are made and are subject to a variety of risks including the risk that the company's products may not perform as expected; that the company may not receive the requisite regulatory market authorization or results of testing; the Company's testing of the products may not be successful and market authorization may not be obtained in the estimated timelines or at all; the company may not be able to generate revenue from its products as expected or at all; the market for the company's products may not be as described in this news release; and various other risk factors identified in the Asep Medical Inc.'s prospectus dated November 9, 2021, and in the company's management discussion and analysis, available for review under the Company's profile at and uncertainties and other factors that could cause actual events or results to differ materially from those projected in the forward-looking statements. Asep Medical Inc. is under no obligation and expressly disclaims any intention or obligation to update or revise any forward-looking statements, whether as a result of new information, future events or otherwise, except as expressly required by applicable law.

前瞻性陳述-
根據適用的證券法,本新聞稿包含某些符合此類聲明含義的“前瞻性聲明”。前瞻性陳述經常使用諸如“預期”、“計劃”、“繼續”、“預期”、“計劃”、“打算”、“相信”、“預期”、“估計”、“可能”、“將會”、“潛在”、“建議”、“定位”等類似詞語,或某些事件或條件“可能”或“將”發生的陳述。這些陳述包括但不限於:我們的敗血癥體外診斷測試的成功臨床測試和它打算申請監管市場授權;公司沒有按計劃獲得監管市場授權或根本沒有獲得監管市場授權;對我們的先導療法進行臨床前研究,期望這將導致快速臨床試驗;用公司的產品識別膿毒症的時間表;潛在的創收機會;公司產品的治療益處;以及關於公司提出的業務計劃的其他聲明。在整個新聞稿中,在得出結論或做出前瞻性陳述中包含的預測時使用了各種假設。前瞻性陳述是以陳述發表之日管理層的意見和估計為基礎的,可能會受到各種風險的影響,包括公司的產品可能沒有達到預期的表現;公司可能得不到必要的監管市場授權或測試結果;公司對產品的測試可能不成功,可能在估計的時間內無法獲得市場授權或根本無法獲得市場授權;公司可能無法從其產品中獲得預期的收入或根本無法從產品中獲得收入;公司產品的市場可能與本新聞稿中描述的不同;以及在ASEP醫療公司的S招股說明書中確定的各種其他風險因素2021年11月9日,以及公司管理層的討論和分析,以供在公司簡介中審查,以及可能導致實際事件或結果與前瞻性陳述中預測的大不相同的不確定因素和其他因素。除適用法律明確要求外,ASEP Medical Inc.沒有義務更新或修改任何前瞻性陳述,無論是由於新資訊、未來事件還是其他原因。

ENDNOTES
1. Renick, P., Tang, L. (2020). Device-Related Infections. In: Li, B., Moriarty, T., Webster, T., Xing, M. (eds) Racing for the Surface. Springer, Cham.
2 Eby EL, Bengtson LGS, Johnson MP, Burton ML, Hinnenthal J. Economic impact of cardiac implantable electronic device infections: cost analysis at one year in a large U.S. health insurer. J Med Econ. 2020 Jul;23(7):698-705. doi: 10.1080/13696998.2020.1751649. Epub 2020 Apr 22. PMID: 32255386
3. Research and Markets: Medical Device Coatings Market 2023
4. Research and Markets: Medical Device Coatings Market 2023

附註
1.雷尼克,P.,唐,L.(2020)。與設備相關的感染。收錄於:Li,B.,莫裡亞蒂,T.,韋伯斯特,T.,邢某,M.(編輯)《地表賽車》。斯普林格,查姆。
2.Eby El,Bengtson LGS,Johnson MP,Burton ML,Hinnenthal J.心臟可植入電子設備感染的經濟影響:一家美國大型健康保險公司一年的成本分析。J Med Econ。2020年7月;23(7):698-705。DOI:10.1080/13696998.2020.1751649。EPub 2020年4月22日PMID:32255386
3.研究與市場:2023年醫療器械塗料市場
4.研究與市場:2023年醫療器械塗料市場

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