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Cryoport Enters Into Strategic Relationship With Takeda's BioLife Plasma Services

Cryoport Enters Into Strategic Relationship With Takeda's BioLife Plasma Services

Cryoport公司与武田的BioLife血浆服务建立战略合作关系
PR Newswire ·  2022/09/08 08:41

Cryoport plans to establish an integrated supply chain platform with BioLife Plasma Services to offer standardized cell therapy collection, processing, and storage services in United States and Europe over time

Cryoport计划与BioLife血浆服务公司建立集成供应链平台,以提供标准化的细胞治疗收集、处理和存储服务美国欧洲随着时间的推移

NASHVILLE, Tenn., Sept. 8, 2022 /PRNewswire/ -- Cryoport, Inc. ( Nasdaq: CYRX) ("Cryoport" or the "Company"), a global leader in temperature-controlled supply chain solutions for the life sciences industry, today announced it has entered into a strategic relationship with BioLife Plasma Services, part of the global biopharmaceutical company Takeda, intended to provide consistent, high-quality cellular starting material for use in the manufacture of life-saving cellular therapies.

田纳西州纳什维尔9月2022年8月美通社/--Cryoport公司面向生命科学行业温控供应链解决方案领域的全球领先企业--纳斯达克(以下称“冷冻”或“公司”)今天宣布,公司已与全球生物制药公司武田旗下的BioLife等离子服务公司建立了战略合作伙伴关系,旨在为生产挽救生命的细胞疗法提供始终如一的高质量细胞起始材料。

By bringing together BioLife Plasma Services' proficiency in apheresis collection and their donation center infrastructure with Cryoport's life sciences' world-class capabilities and expertise in temperature-controlled supply chain solutions for the biopharmaceutical industry, the companies aim to establish a standardized, integrated apheresis collection, processing, and distribution solution for cellular therapies. Importantly, the new platform will leverage the cryo-processing expertise of Cell Matters, which Cryoport acquired in late July 2022.

通过将BioLife血浆服务公司在分离收集方面的专长及其捐赠中心基础设施与Cryoport生命科学公司在生物制药行业温控供应链解决方案方面的世界级能力和专业知识相结合,两家公司的目标是为细胞疗法建立标准化的集成分离收集、处理和分销解决方案。重要的是,新平台将利用Cell Matters的冷冻处理专业知识,该公司于2022年7月下旬被Cryoport收购。

Today, the availability of cellular therapy assets is limited by inflexibility in donation scheduling, a lack of standardization in collection and processing, and challenges inherent towards ensuring compliance with the Good Manufacturing Process (GMP) regulations. This new relationship, which will facilitate strict compliance with applicable GMP regulations, aims to shorten processing and logistics time and standardize collections, contracting, and equipment, in turn, enabling researchers and developers to accelerate cellular therapy programs. Increased access to apheresis, with efficient, scalable and reliable end-to-end processes will benefit not only donors and patients, but manufacturers and the providers of these life-saving therapies. 

今天,细胞治疗资产的可用性受到捐赠时间表缺乏灵活性、收集和处理缺乏标准化以及确保遵守良好制造工艺(GMP)法规的内在挑战的限制。这一新的关系将促进严格遵守适用的GMP法规,旨在缩短加工和物流时间,并标准化收集、承包和设备,从而使研究人员和开发人员能够加快细胞治疗计划。通过高效、可扩展和可靠的端到端过程,增加获得分离的机会,这不仅将使捐赠者和患者受益,而且将使制造商和这些挽救生命的疗法的提供者受益。

Commenting on the agreement, Jerrell Shelton, Chief Executive Officer of Cryoport stated, "This strategic relationship with BioLife Plasma Services is a prime example of how our world-class expertise in providing supply chain solutions to the life sciences industry and our expansion into new geographies and services offerings, such as bioservices and cryo-processing, creates exciting new opportunities. Our goal is to streamline the complex processes necessary to treat an increasing number of patients with today's most advanced cell therapies while ensuring the highest quality and safety standards."

在评论这项协议时,Cryoport首席执行官Jerrell Shelton表示:“与BioLife血浆服务公司的战略合作关系是我们在为生命科学行业提供供应链解决方案方面的世界级专业知识以及我们向生物服务和冷冻加工等新地区和服务产品的扩展如何创造令人兴奋的新机会的最好例证。我们的目标是简化用当今最先进的细胞疗法治疗越来越多的患者所需的复杂流程,同时确保最高的质量和安全标准。”

As a first step, the two companies will establish a new operating platform in Houston, Texas, that will provide end-to-end collection, processing, and distribution services by bringing together Cryoport's new Houston-based global supply chain center with BioLife Plasma Services' local donation facilities. Under the leadership of BioLife employees trained in and with extensive knowledge of the fields of cellular therapy and apheresis, cellular collections will be performed by dedicated cellular collection staff in a designated space within the BioLife Plasma Services donation center. With immediate effect, the companies will co-operate in strategic business and marketing activities, with the intent of attracting and building a pipeline of customer demand that will utilize the offering. This will provide the opportunity to define infrastructure and capital commitments required to scale up and potentially expand the offering throughout the United States and Europe over time. 

作为第一步,两家公司将在德克萨斯州休斯顿建立一个新的运营平台,通过将Cryoport的新产品整合在一起,提供端到端的收集、处理和分发服务休斯敦总部设在全球供应链中心,拥有BioLife血浆服务公司的当地捐赠设施。在接受过细胞治疗和分离领域培训并具有广泛知识的BioLife员工的领导下,细胞收集将由专门的细胞收集人员在BioLife血浆服务捐赠中心的指定空间内进行。从即日起,两家公司将在战略业务和营销活动方面进行合作,目的是吸引和建立一条利用这一产品的客户需求渠道。这将提供机会来定义扩大规模所需的基础设施和资本承诺,并有可能在全美范围内扩大服务范围。欧洲随着时间的推移。

Hema Tallman, Global Head of BioLife Plasma Services added, "Cell therapy is one of the most promising areas of development in healthcare today. This agreement reflects BioLife Plasma Services' and Takeda's transformative leadership and commitment to bringing better health and a brighter future to patients worldwide. As we are constantly exploring how we might serve unmet patient needs, this relationship will optimize the use of our first-class facilities, industry-leading capabilities and our skilled workforce of medical professionals and technicians. The operational synergy between plasmapheresis and leukopheresis combined with Cryoport's leading flexible cryogenic logistics solutions, uniquely positions the two companies to implement and potentially scale a market-leading end-to-end offering across our global donation center network that could enable more patients to benefit from these life-saving therapies."

生物生命血浆服务全球负责人Hema Tallman补充说:“细胞疗法是当今医疗保健领域最有前途的发展领域之一。这项协议反映了BioLife血浆服务公司和武田公司具有变革性的领导能力,并致力于为全球患者带来更好的健康和更光明的未来。随着我们不断探索如何满足未得到满足的患者需求,这一关系将优化我们一流的设施、行业领先的能力以及我们熟练的医疗专业人员和技术人员队伍的使用。血浆分离和白细胞分离之间的业务协同与Cryoport领先的灵活低温物流解决方案相结合,使两家公司处于独特的地位,能够在我们的全球捐赠中心网络中实施并有可能扩大市场领先的端到端产品,使更多的患者能够从这些挽救生命的疗法中受益。“

Operations are expected to begin in 2022 with apheresis scheduling and collections to be initiated by BioLife Plasma Services in the Houston area. Cryoport will provide cold chain solutions inclusive of packaging, logistics, data management, consulting, program management, cryo-processing, and bioservices.

业务预计将于2022年开始,分离计划和收集将由生物生命血浆服务公司在休斯顿地区启动。Cryoport将提供冷链解决方案,包括包装、物流、数据管理、咨询、项目管理、低温加工和生物服务。

About Cryoport, Inc.
关于Cryoport公司

Cryoport, Inc. ( Nasdaq: CYRX), headquartered in Nashville, TN, is a global leader in temperature-controlled supply chain solutions for the life sciences industry supporting life-saving cell and gene therapies across the clinical and commercial spectrum. With 38 strategic locations covering the Americas, EMEA (Europe, the Middle East and Africa) and APAC (Asia Pacific), Cryoport's global platform provides mission-critical solutions, services, and products to Biopharma, Reproductive Medicine, and Animal Health customers worldwide. In addition to its standard setting supply chain solutions, Cryoport is the world's largest manufacturer of cryogenic systems and one of the largest life science focused specialty couriers. As of July 31, 2022, Cryoport supported nine commercial cell and gene therapies and 626 regenerative medicine clinical trials in over 150 countries with 81 of these trials in Phase 3.

总部设在田纳西州纳什维尔的Cryoport公司(纳斯达克代码:CYRX)是生命科学行业温控供应链解决方案的全球领先企业,支持临床和商业领域的挽救生命的细胞和基因疗法。EMEA(EMEA:行情)拥有覆盖美洲的38个战略地点(欧洲、中东和非洲)和亚太地区,Cryoport的全球平台为全球的Biophma、生殖医学和动物健康客户提供关键任务的解决方案、服务和产品。除了制定标准的供应链解决方案外,Cryoport还是世界上最大的低温系统制造商和最大的专注于生命科学的专业快递公司之一。自.起2022年7月31日,Cryoport支持了150多个国家和地区的9种商业细胞和基因疗法以及626项再生医学临床试验,其中81项试验处于第三阶段。

For more information, visit or follow @cryoport on Twitter at for live updates.

欲了解更多信息,请访问或关注Twitter上的@Cryoport:以获取实时更新。

Forward-Looking Statements
前瞻性陈述

Statements in this press release which are not purely historical, including statements regarding the Company's intentions, hopes, beliefs, expectations, representations, projections, plans or predictions of the future, are forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. These forward-looking statements include, but are not limited to, those related to the Company's industry, business, long-term growth prospects, plans, strategy, acquisitions, future financial results and financial condition, such as the Company's outlook and guidance for full year 2022 revenue and the related factors expected to drive revenue, projected trends in the markets in which the Company operates, the Company's intention to expand overall manufacturing capacities, the Company's plan for a new Global Supply Chain Center in Paris, the Company's repurchases of shares of its common stock, and regulatory approvals with respect to the products of the Company's clients. It is important to note that the Company's actual results could differ materially from those in any such forward-looking statements. Factors that could cause actual results to differ materially include, but are not limited to, risks and uncertainties associated with the effect of changing economic conditions, including as a result of the COVID-19 pandemic and its variants, supply chain constraints, inflationary pressures and the effects of foreign currency fluctuations, trends in the products markets, variations in the Company's cash flow, market acceptance risks, and technical development risks. The Company's business could be affected by a number of other factors, including the risk factors discussed in the Company's Securities and Exchange Commission ("SEC") reports including, but not limited to, the Company's Annual Report on Form 10-K for the year ended December 31, 2021, its Quarterly Reports on Form 10-Q filed with the SEC during 2022, as well as in its subsequent filings with the SEC. The forward-looking statements contained in this press release speak only as of the date hereof and the Company cautions investors not to place undue reliance on these forward-looking statements. Except as required by law, the Company disclaims any obligation, and does not undertake to update or revise any forward-looking statements in this press release.

本新闻稿中非纯粹历史性的陈述,包括有关公司的意图、希望、信念、期望、陈述、预测、计划或对未来的预测的陈述,都是符合1995年私人证券诉讼改革法的前瞻性陈述。这些前瞻性陈述包括但不限于与公司的行业、业务、长期增长前景、计划、战略、收购、未来财务结果和财务状况有关的陈述,例如公司对2022年全年收入的展望和指导以及预期推动收入的相关因素、公司经营市场的预测趋势、公司扩大整体制造能力的意图、公司在巴黎建立新的全球供应链中心的计划、公司回购其普通股,以及对公司客户产品的监管批准。值得注意的是,该公司的实际结果可能与任何此类前瞻性陈述中的结果大不相同。可能导致实际结果大不相同的因素包括但不限于与经济状况变化的影响有关的风险和不确定因素,包括新冠肺炎及其变种的影响、供应链限制、通胀压力和外汇波动的影响、产品市场的趋势、公司现金流的变化、市场接受风险和技术开发风险。公司的业务可能会受到许多其他因素的影响,包括公司的证券交易委员会(“美国证券交易委员会”)报告中讨论的风险因素,包括但不限于公司的截至10-K表格的年度报告2021年12月31日,其在2022年提交给美国证券交易委员会的10-Q表格季度报告,以及在随后提交给美国证券交易委员会的文件中。本新闻稿中包含的前瞻性陈述仅代表截至本新闻稿之日的情况,公司告诫投资者不要过度依赖这些前瞻性陈述。除法律另有规定外,公司不承担任何义务,也不承诺更新或修改本新闻稿中的任何前瞻性陈述。

SOURCE Cryoport, Inc.

来源Cryoport,Inc.

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