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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. 获得不列颠哥伦比亚大学颁发的开创性医疗器械涂层技术的全球独家许可
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").

温哥华,卑诗省2023年7月31日/cnw/-Asep Medical Holdings Inc.(“ASEP Inc.“或”公司“)(CSE:ASEP)(场外交易市场:SEPSF)(法兰克福证券交易所:JJ8)高兴地宣布,截至2023年7月21日,它已经完成了收购SafeCoat Medical Inc.的最后一个里程碑。安全涂层“)并签订独家全球许可协议(”协议“)与不列颠哥伦比亚大学(“UBC),通过其子公司SafeCoat,用于使用、开发和商业化突破性的医疗器械涂层技术(技术“)。

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

与设备相关的感染占所有与医疗保健相关的感染的四分之一,由于设备表面的细菌生物膜的黏附和生长,很难用常规抗生素治疗。导尿管是可能导致严重感染的医疗器械的一个很好的例子。根据疾病控制和预防中心(CDC)的数据,大约90%由导管引起的严重感染与中心静脉导管(CVCs)有关。CVC感染不仅对患者来说是严重的,而且对医院来说也是昂贵的,因为每次感染的成本估计从34,508美元56,000美元。这意味着每年护理这些患者的成本约为美元。2.96亿美元-仅在美国就有23亿美元。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.

该技术包括两个关键方面,以防止与设备相关的感染,这会导致额外的成本57,000美元2.并且需要更换受感染的设备。该涂层包括连接到设备表面以杀灭细菌的抗菌肽,以及防止死亡细菌结合到设备表面并掩盖杀菌效果的防污染自组装聚合物。这种涂层技术可以应用于外科植入物、导管、起搏器、支架、假肢和器官以及隐形眼镜上的各种表面,包括玻璃、塑料和钛。动物模型已经证明了这种方法的可行性。与设备相关的感染占所有与医疗保健相关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:

根据研究和市场医疗器械涂料:全球市场报告称,2022年医疗器械涂层的估计价值为美元58亿美元预计将增长到美元97亿美元到2027年,复合年增长率(CAGR)为10.9%3.。该报告还为市场的增长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
  • 人口老龄化正在推动对医疗器械的需求增加
  • 技术的进步导致了需要涂层的新医疗器械的开发
  • 心脏病和糖尿病等慢性病发病率的上升推动了对可用于长期治疗的医疗设备的需求
  • 随着科学技术的进步,FDA和其他监管机构制定了严格的要求,通过改善医疗器械的安全性和性能来提高患者的安全性,这导致了对能够满足这些要求的涂料的需求增加
  • 从长远来看,医疗器械涂层可以通过延长设备的寿命或减少频繁更换的需要来实现成本效益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.

我们很高兴通过SafeCoat Medical和UBC的独家全球许可来推动这项前景光明的新技术的发展。我们预计,随着我们解决医疗器械和植入物的无菌表面维护问题,这笔交易将创造重要的新市场机会。蒂姆·墨菲、Asep Inc.首席运营官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.

根据协议,ASEP公司将持有SafeCoat公司88%的已发行和流通股。作为授予独家许可的代价,UBC和该技术的非放弃发明者将共同拥有SafeCoat剩余12%的已发行和流通股。Dr。罗伯特·W·汉考克,Asep Inc.的创始人兼首席执行官,是SafeCoat技术的四位不放弃发明者之一。

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.

本协议的有效期将在授予许可证和与该技术有关的最后一项专利的到期日起20年后到期。作为授予许可的代价,SafeCoat将向UBC支付从SafeCoat将技术产品商业化所产生的收入的特许权使用费,费率为3.75%,并按照协议中特别规定的分许可阶段性更高的费率支付。SafeCoat还将于****年向UBC支付年费1月1日每一年的数目如下:5,000美元从2024年到2026年,1万美元从2027年到2029年,15,000美元从2030年到2032年,5万美元自2033年起及其后每一年。SafeCoat还将进行里程碑式的付款150,000美元根据技术获得510(K)许可或PMA(如果在美国以外,则为同等产品)的每个产品提交UBC批准。SafeCoat还需要向UBC支付某些专利管理费。

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.

本公司首席执行官兼董事成员汉考克博士是许可协议的订约方,因为他是非放弃发明人之一;因此,与汉考克博士的交易部分被视为多边文书61-101《在特殊交易中保护少数股权持有人》所指的“关联方”(“米其林61-101),而拟向Hancock博士发行本公司子公司SafeCoat Medical Inc.的普通股,被认为是MI 61-101所指的“关联方交易”。该等关联方交易因第5.5(B)节所载豁免而获豁免遵守MI 61-101的估值规定,而由于本公司的股份并非于指定市场上市而获豁免遵守MI 61-101的小股东批准规定,以及凭借MI 61-101第5.7(A)节所载的豁免而获豁免遵守MI 61-101的小股东批准规定,即将向各关联方发行的股份代价的公平市价不超过本公司市值的25%。

ABOUT ASEP MEDICAL HOLDINGS INC.

Asep医疗控股公司简介

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.()致力于通过为人类医学中未得到满足的重大医疗需求开发新的解决方案来解决抗生素失效的全球问题。该公司是由三家现有的私营公司合并而成的,它们的技术都处于高级开发阶段--Sepset Biosciences Inc.(能够及早及时识别脓毒症的专有诊断工具)、ABT Innovation Inc.(用于解决多重耐药生物膜感染的广谱治疗剂)和SafeCoat Medical Inc.(一种抗菌肽医疗设备涂层技术)。

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.

赛普塞特生物科学公司。()正处于临床研究和体外诊断测试商业化的最后阶段,该测试涉及患者基因表达签名,有助于评估严重脓毒症的发展,这是导致抗生素失效的重大疾病之一,因为抗生素是脓毒症的主要初始治疗方法。2017年,脓毒症占全球死亡人数的近20%,几乎所有死于新冠肺炎和其他流行病的人都死于败血症。SepsetER测试是一种基于血液的基因表达测试,操作简单,在急诊室或重症监护病房采集血液样本约一小时后即可获得结果。这项专利诊断技术不同于目前的诊断测试,可以在启动测试后约60分钟内对进展为严重脓毒症的风险进行评估。细菌培养是金标准,大约15小时后就会产生结果,但可能长达3天。ASEP公司相信,它的测试将使医生能够就适当的治疗做出关键的早期决定,从而降低因脓毒症而导致的总体发病率和死亡率。

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创新公司的S()多肽技术涵盖广泛的治疗应用,包括细菌生物被膜感染(牙科、伤口、鼻窦炎、皮肤、医疗器械感染、慢性感染、肺、膀胱、耳鼻喉科、骨科等)、抗炎药物、抗感染免疫调节剂和疫苗佐剂。该公司正处于临床前开发阶段,前三个适应症的数据前景看好。

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医疗公司的S()技术包括防污自组装聚合物和结合在一起的抗菌肽,这些抗菌肽可以作为抗菌和防污涂层应用于各种表面。具体地,本发明涉及可应用于多种医疗设备和植入物的涂层,并且已经在动物模型中证明了可行性。该公司的专业知识还包括制造和应用这些抗菌涂料的方法。

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.

前瞻性陈述-
根据适用的证券法,本新闻稿包含某些符合此类声明含义的“前瞻性声明”。前瞻性陈述经常使用诸如“预期”、“计划”、“继续”、“预期”、“计划”、“打算”、“相信”、“预期”、“估计”、“可能”、“将会”、“潜在”、“建议”、“定位”等类似词语,或某些事件或条件“可能”或“将”发生的陈述。这些陈述包括但不限于:我们的败血症体外诊断测试的成功临床测试和它打算申请监管市场授权;公司没有按计划获得监管市场授权或根本没有获得监管市场授权;对我们的先导疗法进行临床前研究,期望这将导致快速临床试验;用公司的产品识别脓毒症的时间表;潜在的创收机会;公司产品的治疗益处;以及关于公司提出的业务计划的其他声明。在整个新闻稿中,在得出结论或做出前瞻性陈述中包含的预测时使用了各种假设。前瞻性陈述是以陈述发表之日管理层的意见和估计为基础的,可能会受到各种风险的影响,包括公司的产品可能没有达到预期的表现;公司可能得不到必要的监管市场授权或测试结果;公司对产品的测试可能不成功,可能在估计的时间内无法获得市场授权或根本无法获得市场授权;公司可能无法从其产品中获得预期的收入或根本无法从产品中获得收入;公司产品的市场可能与本新闻稿中描述的不同;以及在ASEP医疗公司的S招股说明书中确定的各种其他风险因素2021年11月9日,以及公司管理层的讨论和分析,以供在公司简介中审查,以及可能导致实际事件或结果与前瞻性陈述中预测的大不相同的不确定因素和其他因素。除适用法律明确要求外,ASEP Medical Inc.没有义务更新或修改任何前瞻性陈述,无论是由于新信息、未来事件还是其他原因。

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

尾注
1.雷尼克,P.,唐,L.(2020)。与设备相关的感染。收录于:Li,B.,莫里亚蒂,T.,韦伯斯特,T.,邢某,M.(编辑)《地表赛车》。斯普林格,查姆。
2.Eby El,Bengtson LGS,Johnson MP,Burton ML,Hinnenthal J.心脏可植入电子设备感染的经济影响:一家美国大型健康保险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.研究与市场:2023年医疗器械涂料市场
4.研究与市场:2023年医疗器械涂料市场

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