{"id":440554,"date":"2026-10-21T20:40:15","date_gmt":"2026-10-21T13:40:15","guid":{"rendered":"https:\/\/www.swingfish.trade\/blog\/market-news\/inmune-bio-establishes-global-commercialization-framework-for-ebstrocel-through-strategic-agreement-with-uniphar-440554\/"},"modified":"2026-10-21T20:40:15","modified_gmt":"2026-10-21T13:40:15","slug":"inmune-bio-establishes-global-commercialization-framework-for-ebstrocel-through-strategic-agreement-with-uniphar","status":"publish","type":"post","link":"https:\/\/www.swingfish.trade\/blog\/market-news\/inmune-bio-establishes-global-commercialization-framework-for-ebstrocel-through-strategic-agreement-with-uniphar-440554\/","title":{"rendered":"INmune Bio Establishes Global Commercialization Framework for Ebstrocel\u2122 Through Strategic Agreement with Uniphar"},"content":{"rendered":"<div>\n<p class=\"MsoNormal\" style=\"margin: 0 0 11px;line-height: 115%;font-size: 16px;font-family: Aptos, sans-serif\">INmune Bio Inc.<br \/>\n        (NASDAQ: INMB) (the \u201cCompany\u201d), a late-stage biotechnology company focused on<br \/>\n        inflammation and immunology, today announced that it has entered into a Master<br \/>\n        Services Agreement with Uniphar Durbin Ireland Limited (\u201cUniphar\u201d) establishing<br \/>\n        a scalable framework to support international access, distribution and<br \/>\n        commercialization of Ebstrocel\u2122, the Company\u2019s allogeneic stromal cell therapy<br \/>\n        for Recessive Dystrophic Epidermolysis Bullosa (RDEB). INmune Bio initially<br \/>\n        intends to use the framework to pursue named-patient access in selected<br \/>\n        European countries and in the Middle East and North Africa (MENA), subject to<br \/>\n        applicable law and country-specific statements of work. The relationship may<br \/>\n        subsequently expand across Europe and other territories by mutual agreement.<\/p>\n<p class=\"MsoNormal\" style=\"margin: 0 0 11px;line-height: 115%;font-size: 16px;font-family: Aptos, sans-serif\">The Company expects<br \/>\n        named-patient access to be an important component of its international<br \/>\n        commercialization strategy for Ebstrocel\u2122. Where permitted by local law and<br \/>\n        implemented through statements of work, this pathway may allow physicians to<br \/>\n        request Ebstrocel\u2122 for individual eligible patients before local marketing<br \/>\n        approval or broad commercial availability.<\/p>\n<p class=\"MsoNormal\" style=\"margin: 0 0 11px;line-height: 115%;font-size: 16px;font-family: Aptos, sans-serif\">The Uniphar framework<br \/>\n        is designed to provide the Company with scalable international commercial<br \/>\n        infrastructure, beginning with named-patient supply, and potentially expanding<br \/>\n        to broader commercial distribution as regulatory approvals, pricing and reimbursement<br \/>\n        are secured in individual countries. Depending on the services agreed in<br \/>\n        individual statements of work, Uniphar may support regulatory feasibility<br \/>\n        assessments, market access, product storage and distribution,<br \/>\n        healthcare-provider and treatment-site onboarding, order-to-cash services,<br \/>\n        medical information, pharmacovigilance support and end-to-end shipment<br \/>\n        tracking. By leveraging Uniphar\u2019s established infrastructure rather than<br \/>\n        building country-by-country capabilities internally, the Company believes this<br \/>\n        model provides a capital-efficient path to establish Ebstrocel\u2122\u2019s international<br \/>\n        commercial footprint and scale as additional markets become available.<\/p>\n<p class=\"MsoNormal\" style=\"margin: 0 0 11px;line-height: 115%;font-size: 16px;font-family: Aptos, sans-serif\">\u201cThis agreement marks<br \/>\n        an important step in moving Ebstrocel\u2122 from clinical development toward<br \/>\n        commercialization and bringing Ebstrocel to patients internationally,\u201d said<br \/>\n        David Moss, Chief Executive Officer of INmune Bio. \u201cUniphar provides access to<br \/>\n        established market-access, distribution and order-to-cash capabilities across<br \/>\n        multiple international markets without requiring INmune Bio to build those<br \/>\n        capabilities country by country. We believe this provides a capital-efficient<br \/>\n        way to pursue named-patient opportunities in appropriate markets while building<br \/>\n        the physician relationships, treatment-center experience and commercial<br \/>\n        infrastructure needed to support broader international<br \/>\n        commercialization.\u201d\u00a0\u201cWe are pleased to partner with INmune Bio as it<br \/>\n        prepares Ebstrocel for international commercialization,\u201d said Ruth Rostron,<br \/>\n        Head of Expanded Access at Uniphar. \u201cUniphar has built an integrated global<br \/>\n        platform to help innovative medicines navigate the complexities of<br \/>\n        international access, distribution and commercialization. We believe our<br \/>\n        infrastructure and experience are well suited to support INmune Bio\u2019s strategy<br \/>\n        for Ebstrocel, beginning with named-patient access opportunities and expanding<br \/>\n        as the product progresses through its regulatory and commercial journey.\u201d<\/p>\n<p class=\"MsoNormal\" style=\"margin: 0 0 11px;line-height: 115%;font-size: 16px;font-family: Aptos, sans-serif\">About Ebstrocel\u2122<\/p>\n<p class=\"MsoNormal\" style=\"margin: 0 0 11px;line-height: 115%;font-size: 16px;font-family: Aptos, sans-serif\">Ebstrocel\u2122 (pobistrocel)<br \/>\n        is INmune Bio\u2019s investigational, pooled, allogeneic, human umbilical<br \/>\n        cord-derived mesenchymal stromal cell therapy being developed through the<br \/>\n        Company\u2019s CORDStrom\u2122 platform for the treatment of RDEB. The platform is<br \/>\n        designed to address donor variability and manufacturing inconsistency.<br \/>\n        Ebstrocel\u2122 is investigational and has not been approved by the FDA, MHRA, EMA<br \/>\n        or any other regulatory authority.<\/p>\n<p class=\"MsoNormal\" style=\"margin: 0 0 11px;line-height: 115%;font-size: 16px;font-family: Aptos, sans-serif\">About Uniphar Plc.<\/p>\n<p class=\"MsoNormal\" style=\"margin: 0 0 11px;line-height: 115%;font-size: 16px;font-family: Aptos, sans-serif\">Uniphar is a trusted<br \/>\n        global partner to pharma, medtech and biotech, delivering solutions that<br \/>\n        connect medicines and technologies with patients worldwide. With over 57 years<br \/>\n        of experience and partnerships with 200+ multinational clients, Uniphar<br \/>\n        combines deep expertise, global infrastructure and market insight to meet the<br \/>\n        evolving needs of the life sciences sector.<\/p>\n<p class=\"MsoNormal\" style=\"margin: 0 0 11px;line-height: 115%;font-size: 16px;font-family: Aptos, sans-serif\">Uniphar Pharma<br \/>\n        integrates Development, Clinical, Access, Medical, Commercial, Distribution and<br \/>\n        Global Sourcing to support the full product lifecycle \u2013 from early-stage<br \/>\n        research through to commercialization and beyond. Uniphar\u2019s unified platform<br \/>\n        spans regulatory strategy, clinical trial support, medical affairs, market<br \/>\n        access, patient engagement, commercial services, distribution and supply chain.<\/p>\n<p class=\"MsoNormal\" style=\"margin: 0 0 11px;line-height: 115%;font-size: 16px;font-family: Aptos, sans-serif\">Operating across 160<br \/>\n        countries with a global team of 3,600+, Uniphar bridges manufacturers,<br \/>\n        healthcare providers, and patients \u2014 accelerating access to innovative<br \/>\n        therapies, improving patient outcomes, and delivering value across the<br \/>\n        healthcare ecosystem.<\/p>\n<p class=\"MsoNormal\" style=\"margin: 0 0 11px;line-height: 115%;font-size: 16px;font-family: Aptos, sans-serif\">From molecule to<br \/>\n        market and beyond.<\/p>\n<p class=\"MsoNormal\" style=\"margin: 0 0 11px;line-height: 115%;font-size: 16px;font-family: Aptos, sans-serif\">About INmune Bio<br \/>\n            Inc.<\/p>\n<p class=\"MsoNormal\" style=\"margin: 0 0 11px;line-height: 115%;font-size: 16px;font-family: Aptos, sans-serif\">INmune Bio Inc. https:\/\/www.inmunebio.com\/ is a<br \/>\n        publicly traded (NASDAQ: INMB), late-stage biotechnology company focused on<br \/>\n        developing treatments that target the innate immune system to fight disease.<br \/>\n        Moving beyond early-stage exploration, the Company\u2019s clinical-development<br \/>\n        strategy centers on advanced precision medicine, matching drug mechanisms<br \/>\n        directly to patient biology to optimize clinical outcomes.<\/p>\n<p class=\"MsoNormal\" style=\"margin: 0 0 11px;line-height: 115%;font-size: 16px;font-family: Aptos, sans-serif\">INmune Bio is actively<br \/>\n        advancing two late-stage product platforms toward registrational milestones:<\/p>\n<ul style=\"margin-bottom: 0;margin-top: 0\" type=\"disc\">\n<li class=\"MsoNormal\" style=\"margin: 0 0 11px;line-height: 115%;font-size: 16px;font-family: Aptos, sans-serif\">CORDStrom\u2122: A proprietary, pooled,<br \/>\n            allogeneic, human umbilical cord-derived mesenchymal stromal cell platform<br \/>\n            engineered to address the historical clinical challenges of donor<br \/>\n            variability and manufacturing inconsistency. Following successful clinical<br \/>\n            readouts in RDEB, the platform is transitioning toward regulatory and<br \/>\n            commercial readiness, with an MAA planned for the UK MHRA in 2026 and EU<br \/>\n            EMA in 2027, alongside a planned U.S. regulatory pathway and development<br \/>\n            of international access and distribution infrastructure.<\/li>\n<li class=\"MsoNormal\" style=\"margin: 0 0 11px;line-height: 115%;font-size: 16px;font-family: Aptos, sans-serif\">XPro1595\u2122: A Dominant-Negative Tumor<br \/>\n            Necrosis Factor (DN-TNF) platform that selectively neutralizes soluble TNF<br \/>\n            (sTNF) to reduce pathological neuroinflammation without compromising<br \/>\n            protective immune function. Backed by recently granted FDA Fast Track designation<br \/>\n            and successful regulatory alignment from an End-of-Phase 2 meeting,<br \/>\n            XPro1595\u2122 is positioned for an integrated Phase 2b\/3 seamless adaptive<br \/>\n            registrational program in neuroinflammation-enriched early Alzheimer\u2019s<br \/>\n            disease.<\/li>\n<\/ul>\n<p class=\"MsoNormal\" style=\"margin: 0 0 11px;line-height: 115%;font-size: 16px;font-family: Aptos, sans-serif\">To learn more about<br \/>\n        INmune Bio\u2019s pipeline and its approach to harnessing the innate immune system,<br \/>\n        please visit <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=tFru9cwnyCYUvuuPbUFL9s-BcCYoXl0Z_UydZyV9mzKw43grvR3Vg05xGFQPdxnrQKuIlI3EHqOiPhAOGec4VSmy6vZFh2VnUNTT9X-yw0Y%3D\" style=\"text-decoration: underline\" rel=\"follow\">www.inmunebio.com<\/a>.<\/p>\n<p class=\"MsoNormal\" style=\"margin: 0 0 11px;line-height: 115%;font-size: 16px;font-family: Aptos, sans-serif\">Forward Looking<br \/>\n            Statements<\/p>\n<p class=\"MsoNormal\" style=\"margin: 0 0 11px;line-height: 115%;font-size: 16px;font-family: Aptos, sans-serif\">The Company\u2019s product<br \/>\n        candidates are investigational, and there can be no assurance that any<br \/>\n        clinical, regulatory or commercial objective will be achieved. Any statements<br \/>\n        contained in this press release related to the development or commercialization<br \/>\n        of product candidates and other business and financial matters, including<br \/>\n        without limitation, trial results and data, timing of key milestones, future<br \/>\n        plans or expectations, the scope and implementation of the Uniphar relationship,<br \/>\n        the execution of statements of work, the availability and timing of<br \/>\n        named-patient or expanded-access sales, potential revenue, potential expansion<br \/>\n        across Europe or into Latin America, the anticipated capital efficiency of the<br \/>\n        distribution model, and the prospects for receiving regulatory approval or<br \/>\n        commercializing or selling any product or drug candidates, may constitute<br \/>\n        forward-looking statements as that term is defined in the Private Securities<br \/>\n        Litigation Reform Act of 1995. Any forward-looking statements contained herein<br \/>\n        are based on current expectations but are subject to several risks and<br \/>\n        uncertainties. Actual results and the timing of certain events and<br \/>\n        circumstances may differ materially from those described by the forward-looking<br \/>\n        statements because of these risks and uncertainties. CORDStrom\u2122 (EbstrocelTM, pobistrocel),<br \/>\n        XPro1595\u2122 (XPro\u2122, pegipanermin), and INKmune\u2122 have either finished clinical<br \/>\n        trials, are still in clinical trials or are preparing to start clinical trials<br \/>\n        and have not been approved by the US Food and Drug Administration (FDA), the UK<br \/>\n        MHRA or any regulatory body and there cannot be any assurance that they will be<br \/>\n        approved by the FDA, the UK MHRA or any regulatory body or that any specific<br \/>\n        results will be achieved. The factors that could cause actual future results to<br \/>\n        differ materially from current expectations include, but are not limited to,<br \/>\n        risks and uncertainties relating to the Company\u2019s ability to produce more drug<br \/>\n        for clinical trials; the availability of substantial additional funding for the<br \/>\n        Company to continue its operations and to conduct research and development,<br \/>\n        clinical studies and future product commercialization; and the Company\u2019s<br \/>\n        business, research, product development, regulatory approval, marketing and<br \/>\n        distribution plans and strategies. These and other factors are identified and<br \/>\n        described in more detail in the Company\u2019s filings with the Securities and<br \/>\n        Exchange Commission, including the Company\u2019s Annual Report on Form 10-K, the<br \/>\n        Company\u2019s Quarterly Reports on Form 10-Q and the Company\u2019s Current Reports on<br \/>\n        Form 8-K. The Company assumes no obligation to update any forward-looking<br \/>\n        statements to reflect any event or circumstance that may arise after the date<br \/>\n        of this release.<\/p>\n<p class=\"MsoNormal\" style=\"margin: 0 0 11px;line-height: 115%;font-size: 16px;font-family: Aptos, sans-serif\">\u00a0<\/p>\n<p>                            This article was written by IL Contributors at investinglive.com.<\/p><\/div>\n","protected":false},"excerpt":{"rendered":"<p>INmune Bio Inc. (NASDAQ: INMB) (the \u201cCompany\u201d), a late-stage biotechnology company focused on inflammation and immunology, today announced that it has entered into a Master Services Agreement with Uniphar Durbin Ireland Limited&hellip;<\/p>\n","protected":false},"author":216,"featured_media":0,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[86],"tags":[],"class_list":["post-440554","post","type-post","status-publish","format-standard","hentry","category-market-news"],"_links":{"self":[{"href":"https:\/\/www.swingfish.trade\/blog\/wp-json\/wp\/v2\/posts\/440554","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.swingfish.trade\/blog\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.swingfish.trade\/blog\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.swingfish.trade\/blog\/wp-json\/wp\/v2\/users\/216"}],"replies":[{"embeddable":true,"href":"https:\/\/www.swingfish.trade\/blog\/wp-json\/wp\/v2\/comments?post=440554"}],"version-history":[{"count":0,"href":"https:\/\/www.swingfish.trade\/blog\/wp-json\/wp\/v2\/posts\/440554\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.swingfish.trade\/blog\/wp-json\/wp\/v2\/media?parent=440554"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.swingfish.trade\/blog\/wp-json\/wp\/v2\/categories?post=440554"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.swingfish.trade\/blog\/wp-json\/wp\/v2\/tags?post=440554"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}