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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公司與武田的BioLife血漿服務建立戰略合作關係
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計劃與BioLife血漿服務公司建立集成供應鏈平臺,以提供標準化的細胞治療收集、處理和存儲服務美國歐洲隨着時間的推移

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.

田納西州納什維爾9月2022年8月美通社/--Cryoport公司面向生命科學行業温控供應鏈解決方案領域的全球領先企業--納斯達克(以下稱“冷凍”或“公司”)今天宣佈,公司已與全球生物製藥公司武田旗下的BioLife等離子服務公司建立了戰略合作伙伴關係,旨在為生產挽救生命的細胞療法提供始終如一的高質量細胞起始材料。

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.

通過將BioLife血漿服務公司在分離收集方面的專長及其捐贈中心基礎設施與Cryoport生命科學公司在生物製藥行業温控供應鏈解決方案方面的世界級能力和專業知識相結合,兩家公司的目標是為細胞療法建立標準化的集成分離收集、處理和分銷解決方案。重要的是,新平臺將利用Cell Matters的冷凍處理專業知識,該公司於2022年7月下旬被Cryoport收購。

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,細胞治療資產的可用性受到捐贈時間表缺乏靈活性、收集和處理缺乏標準化以及確保遵守良好製造工藝(GMP)法規的內在挑戰的限制。這一新的關係將促進嚴格遵守適用的GMP法規,旨在縮短加工和物流時間,並標準化收集、承包和設備,從而使研究人員和開發人員能夠加快細胞治療計劃。通過高效、可擴展和可靠的端到端過程,增加獲得分離的機會,這不僅將使捐贈者和患者受益,而且將使製造商和這些挽救生命的療法的提供者受益。

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."

在評論這項協議時,Cryoport首席執行官Jerrell Shelton表示:“與BioLife血漿服務公司的戰略合作關係是我們在為生命科學行業提供供應鏈解決方案方面的世界級專業知識以及我們向生物服務和冷凍加工等新地區和服務產品的擴展如何創造令人興奮的新機會的最好例證。我們的目標是簡化用當今最先進的細胞療法治療越來越多的患者所需的複雜流程,同時確保最高的質量和安全標準。”

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. 

作為第一步,兩家公司將在德克薩斯州休斯頓建立一個新的運營平臺,通過將Cryoport的新產品整合在一起,提供端到端的收集、處理和分發服務休斯敦總部設在全球供應鏈中心,擁有BioLife血漿服務公司的當地捐贈設施。在接受過細胞治療和分離領域培訓並具有廣泛知識的BioLife員工的領導下,細胞收集將由專門的細胞收集人員在BioLife血漿服務捐贈中心的指定空間內進行。從即日起,兩家公司將在戰略業務和營銷活動方面進行合作,目的是吸引和建立一條利用這一產品的客户需求渠道。這將提供機會來定義擴大規模所需的基礎設施和資本承諾,並有可能在全美範圍內擴大服務範圍。歐洲隨着時間的推移。

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."

生物生命血漿服務全球負責人Hema Tallman補充説:“細胞療法是當今醫療保健領域最有前途的發展領域之一。這項協議反映了BioLife血漿服務公司和武田公司具有變革性的領導能力,並致力於為全球患者帶來更好的健康和更光明的未來。隨着我們不斷探索如何滿足未得到滿足的患者需求,這一關係將優化我們一流的設施、行業領先的能力以及我們熟練的醫療專業人員和技術人員隊伍的使用。血漿分離和白細胞分離之間的業務協同與Cryoport領先的靈活低温物流解決方案相結合,使兩家公司處於獨特的地位,能夠在我們的全球捐贈中心網絡中實施並有可能擴大市場領先的端到端產品,使更多的患者能夠從這些挽救生命的療法中受益。“

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.

業務預計將於2022年開始,分離計劃和收集將由生物生命血漿服務公司在休斯頓地區啟動。Cryoport將提供冷鏈解決方案,包括包裝、物流、數據管理、諮詢、項目管理、低温加工和生物服務。

About Cryoport, Inc.
關於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.

總部設在田納西州納什維爾的Cryoport公司(納斯達克代碼:CYRX)是生命科學行業温控供應鏈解決方案的全球領先企業,支持臨牀和商業領域的挽救生命的細胞和基因療法。EMEA(EMEA:行情)擁有覆蓋美洲的38個戰略地點(歐洲、中東和非洲)和亞太地區,Cryoport的全球平臺為全球的Biophma、生殖醫學和動物健康客户提供關鍵任務的解決方案、服務和產品。除了制定標準的供應鏈解決方案外,Cryoport還是世界上最大的低温系統製造商和最大的專注於生命科學的專業快遞公司之一。自.起2022年7月31日,Cryoport支持了150多個國家和地區的9種商業細胞和基因療法以及626項再生醫學臨牀試驗,其中81項試驗處於第三階段。

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

欲瞭解更多信息,請訪問或關注Twitter上的@Cryoport:以獲取實時更新。

Forward-Looking Statements
前瞻性陳述

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.

本新聞稿中非純粹歷史性的陳述,包括有關公司的意圖、希望、信念、期望、陳述、預測、計劃或對未來的預測的陳述,都是符合1995年私人證券訴訟改革法的前瞻性陳述。這些前瞻性陳述包括但不限於與公司的行業、業務、長期增長前景、計劃、戰略、收購、未來財務結果和財務狀況有關的陳述,例如公司對2022年全年收入的展望和指導以及預期推動收入的相關因素、公司經營市場的預測趨勢、公司擴大整體制造能力的意圖、公司在巴黎建立新的全球供應鏈中心的計劃、公司回購其普通股,以及對公司客户產品的監管批准。值得注意的是,該公司的實際結果可能與任何此類前瞻性陳述中的結果大不相同。可能導致實際結果大不相同的因素包括但不限於與經濟狀況變化的影響有關的風險和不確定因素,包括新冠肺炎及其變種的影響、供應鏈限制、通脹壓力和外匯波動的影響、產品市場的趨勢、公司現金流的變化、市場接受風險和技術開發風險。公司的業務可能會受到許多其他因素的影響,包括公司的證券交易委員會(“美國證券交易委員會”)報告中討論的風險因素,包括但不限於公司的截至10-K表格的年度報告2021年12月31日,其在2022年提交給美國證券交易委員會的10-Q表格季度報告,以及在隨後提交給美國證券交易委員會的文件中。本新聞稿中包含的前瞻性陳述僅代表截至本新聞稿之日的情況,公司告誡投資者不要過度依賴這些前瞻性陳述。除法律另有規定外,公司不承擔任何義務,也不承諾更新或修改本新聞稿中的任何前瞻性陳述。

SOURCE Cryoport, Inc.

來源Cryoport,Inc.

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