Cellares provides automated, closed-system manufacturing and quality control for cell therapies through its Cell Shuttle end-to-end GMP production platform and Cell Q in-process and release testing. These two parts create a linked, automated workflow that can run in dedicated Smart Factories, delivering much higher throughput and lower per-patient costs than traditional CDMOs of similar size. Its approach combines scalable automation, integrated QC, and a global network of facilities, along with partnerships such as Bristol Myers Squibb, and an FDA Advanced Manufacturing Technology designation for its Cell Shuttle. Its goal is to industrialize cell therapy production at scale, reduce costs, and enable broader adoption of cell therapies worldwide.
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Company Size
201-500
Company Stage
Series D
Total Funding
$682M
Headquarters
South San Francisco, CA
Founded
2019
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The Associated Press Sep 23, 2026, 9:00 AM Cellares and Seoul National University Hospital launch proof-of-concept for automated manufacturing of gene-modified HSPC therapy on the Cell Shuttle(R) platform. SOUTH SAN FRANCISCO, Calif.-(BUSINESS WIRE)-Sep 23, 2026- Cellares, the first Integrated Development and Manufacturing Organization (IDMO), and Seoul National University Hospital (SNUH), a leading translational medical center in South Korea, today announced a partnership to evaluate automated manufacturing for a gene-modified hematopoietic stem and progenitor cell (HSPC) therapy targeting paroxysmal nocturnal hemoglobinuria (PNH) on Cellares' Cell Shuttle platform. The collaboration will evaluate the translation of SNUH's gene-modified HSPC manufacturing process to the Cell Shuttle, with a focus on supporting a two-step transfection workflow, through the use of Cellares fully integrated and single-use electroporation module. The partnership marks Cellares' second collaboration in Asia and expands the company's collaboration network in the Asia-Pacific region as it supports SNUH's program toward clinical development in the United States. SNUH is an elite translational medical center that collaborates with leading global institutions on gene-modified hematopoietic stem cell therapies. Through the partnership, Cellares will support preclinical development and IND-enabling manufacturing workflows for SNUH's PNH program, with the goal of establishing a scalable manufacturing strategy for future U.S. clinical development. "Advancing gene-modified HSPC therapies requires a manufacturing approach that can support both the complexity of the process and the rigor of clinical translation," said Professor Youngil Koh, Director of the SNUH GMP Facility. "By working with Cellares, we are evaluating how automation can strengthen manufacturing reliability and scalability as we advance this program toward clinical development." "Gene-modified HSPC therapies are a natural fit for the Cell Shuttle and an area where Cellares has established manufacturing expertise," said Fabian Gerlinghaus, Co-Founder and CEO of Cellares. "By automating complex workflows, including electroporation, we can deliver the scalability, reliability and manufacturing economics required to advance these therapies through clinical development. This partnership extends that capability to SNUH as it prepares its PNH program for future clinical development in the United States." Gene-modified HSC manufacturing remains labor-intensive, variable and difficult to scale, limiting clinical development, increasing manufacturing costs and constraining patient access. The Cell Shuttle is an end-to-end automated cell therapy manufacturing platform designed to improve the scalability and reliability of autologous cell therapy manufacturing. The proof-of-concept will assess the potential to automate SNUH's manufacturing process on the Cell Shuttle, with the goal of improving reliability, driving down manufacturing costs and supporting broader patient access as the program advances. About Cellares Cellares is the first Integrated Development and Manufacturing Organization (IDMO), providing global cell therapy development and manufacturing services through an Industry 4.0 approach to the mass manufacture of the living drugs of the 21st century. The company enables drug sponsors to develop, scale, and commercialize cell therapies with the capacity, reliability, and economics required to meet total patient demand. Cellares' fully automated platforms - Cell Shuttle(R) for end-to-end cell therapy manufacturing and Cell Q(TM) for automated in-process and release quality control - are deployed across its network of IDMO Smart Factories worldwide. These technologies deliver industry-leading manufacturing economics, higher process success rates, and the ability to produce up to 10x more cell therapy batches than conventional CDMOs with comparable footprint and headcount, resulting in the lowest cost of manufacturing in the industry. The Cell Shuttle is the first cell therapy manufacturing platform to receive the FDA's Advanced Manufacturing Technology (AMT) designation, and has demonstrated a 100% automation success rate across more than a dozen automated processes. Cellares was also accepted into the FDA's inaugural Manufacturing PreCheck cohort, the only cell therapy platform among seven companies nationwide, giving Cellares early and ongoing engagement with the FDA during facility development and application submission periods, compressing regulatory timelines and de-risking the path to commercial-scale production for the drug sponsors building on Cellares' platform. Cellares has achieved key clinical validation milestones, including a successful IND Amendment enabling active clinical manufacturing on the Cell Shuttle platform, and the successful dosing of first patients in a partner clinical trial - marking the platform's transition from development-stage technology to clinically validated manufacturing infrastructure. These milestones span multiple therapeutic areas and cell therapy modalities, including both oncology and autoimmune indications. Headquartered in South San Francisco, California, Cellares operates its first commercial-scale IDMO Smart Factory in Bridgewater, New Jersey, with additional facilities under construction in Europe and Japan. Through its global manufacturing network, Cellares is purpose-built to support both clinical and commercial programs and to expand access to life-saving cell therapies worldwide. For more information, visit www.cellares.com and follow Cellares on LinkedIn. About Seoul National University Hospital Seoul National University Hospital (SNUH) is a medical center in South Korea dedicated to advancing patient care through the integration of education, research and clinical practice. SNUH works to advance state-of-the-art medical care and expand knowledge through medical research, while fostering the next generation of global healthcare leaders. As a translational medical center, SNUH also collaborates with leading institutions worldwide on the development of innovative therapies, including gene-modified hematopoietic stem cell-based treatments. Its institutional mission emphasizes excellence across medical care, research and education. Business Development:[email protected] Investors:[email protected] Media:[email protected] National University Hospital Contacts PR Contact:[email protected] KEYWORD: SOUTH KOREA UNITED STATES NORTH AMERICA ASIA PACIFIC CALIFORNIA INDUSTRY KEYWORD: RESEARCH GENERAL HEALTH PHARMACEUTICAL HOSPITALS GENETICS CLINICAL TRIALS SCIENCE BIOTECHNOLOGY STEM CELLS FDA OTHER SCIENCE HEALTH PUB: 09/23/2026 08:00 AM/DISC: 09/23/2026 08:00 AM
Cellares links with GenomeFrontier to test automation approach for virus-free CAR-Ts. Automated manufacturing specialist Cellares is teaming up with Taiwanese biotech GenomeFrontier Therapeutics to evaluate the IDMO's Cell Shuttle platform for production of virus-free CAR-T therapies. The partnership will focus on the compatibility of GenomeFrontier's virus-free manufacturing process with Cellares' Cell Shuttle platform, with the goal of producing the Taiwanese biotech's investigational cell therapy GF-CART01. The CAR-T asset, at phase 1 in its most advanced program, is being developed to treat B-cell malignancies that include diffuse large B-cell lymphoma, follicular lymphoma, primary mediastinal large B-cell lymphoma and high-grade B-cell lymphoma, according to a Sept. 16 release. Unlike today's crop of commercially approved CAR-T therapies that rely on viral vectors, GenomeFrontier is pursuing a virus-free manufacturing approach that research suggests could eliminate manufacturing costs and complexities in the production process, among other potential benefits. Financial details of the collaboration weren't disclosed. The deal, which is Cellares' first development collaboration in Asia, will concentrate on supporting transfection unit operations by leveraging the contract manufacturers' integrated electroporator, which uses electrical pulses to create a physical opening in a cell's membrane. Transfection, meanwhile, refers to the process of introducing other material into those cells. "GenomeFrontier's virus-free approach reflects the increasing complexity of next-generation cell therapy manufacturing," Fabian Gerlinghaus, Cellares' co-founder and chief executive, said in a statement. "The Cell Shuttle is built to automate complex processes, including electroporation-based workflows, with the scalability and reliability needed as therapies advance through clinical development." Cellares touts its Cell Shuttle, roughly the size of a conference room, as a true end-to-end automated manufacturing platform for cell therapies. The technology, which Cellares argues can improve batch yield and success rates while lowering production costs, is paired with the company's companion platform Cell Q for automated in-process and release quality control. News of the partnership comes fast on the heels of Cellares' announced plans to reduce its workforce in California and New Jersey to the tune of about 168 jobs following the loss of a "large pharmaceutical customer." The development was first announced on LinkedIn by Gerlinghaus in August. Multiple sources have since reported the customer was Bristol Myers Squibb, which first linked up with Cellares in 2024 as part of a deal then potentially worth $380 million.
Bristol Myers Squibb ends $380 million Cellares CAR-T manufacturing partnership. BMS concluded that Cellares' automated Cell Shuttle platform could not meet the specific requirements for commercial Breyanzi production, prompting Cellares to cut around 100 positions. Bristol Myers Squibb has terminated its manufacturing partnership with Cellares after determining that the Cell Shuttle automated manufacturing system could not meet the requirements necessary to produce commercial batches of its approved CAR-T therapy Breyanzi (lisocabtagene maraleucel). The termination ends a global capacity reservation and supply agreement originally valued at up to $380 million and has led Cellares to plan approximately 100 job cuts as it resizes its operations. | Field | Content | | Alert Type | Industry Update | | Topic | Cell therapy manufacturing; Partnership termination; Workforce | | Organisation(s) | Bristol Myers Squibb (BMS); Cellares | | Affected Stakeholders | Cellares employees; BMS cell therapy manufacturing operations; CAR-T manufacturing partners | | Therapy Area(s) | Oncology; Haematology; Cell therapy | | Geography | United States | | What Happened | BMS has ended its partnership with Cellares following an evaluation of the Cell Shuttle automated cell therapy manufacturing platform for production of Breyanzi. BMS said the system could not meet the necessary requirements for manufacturing commercial Breyanzi and stressed that its conclusion was specific to Breyanzi and the therapy's established, regulatory-approved manufacturing process. Cellares said it strongly disagrees with BMS's characterisation and noted that Cell Shuttle has produced GMP drug product for an FDA-regulated clinical programme. The companies originally entered a global capacity reservation and supply agreement in 2024 valued at up to $380 million. (BioSpace) | | Why It Matters | The termination illustrates the practical difficulty of introducing a different manufacturing platform for an already approved autologous cell therapy with an established regulatory manufacturing process. For Cellares, the loss is commercially significant because BMS represented a major Cell Shuttle partnership; for BMS, the decision means Breyanzi production will continue without the planned Cellares manufacturing route. (BioSpace) | | Supporting Context | Cell Shuttle is designed to automate end-to-end CAR-T manufacturing at clinical and commercial scale. BMS entered the Cellares agreement in 2024 as part of its manufacturing strategy, while Breyanzi has been FDA approved since 2021 and is currently produced through BMS facilities and specialist external manufacturers. (BioSpace) | | Who Is Most Affected | Cellares and its workforce face the most immediate impact. A California WARN filing indicates that the company plans to permanently eliminate approximately 100 positions on 20 October 2026, spanning engineering, commercial operations, recruitment, software and other functions. (BioSpace) | | Industry Impact | The setback highlights a key challenge for cell therapy manufacturing: technologies designed to automate and scale production must still fit the specific manufacturing and regulatory requirements attached to individual therapies. BMS emphasised that its decision relates specifically to Breyanzi, so it should not be interpreted as establishing that Cell Shuttle is unsuitable for other cell therapy programmes. (BioSpace) | | Key Takeaway | BMS's decision ends a major commercial validation opportunity for Cellares' automated manufacturing platform and shows the barriers involved in changing production processes for an already approved CAR-T therapy. | | What to Watch | Cellares' implementation of the approximately 100 planned job cuts, whether the company secures additional commercial-scale manufacturing customers and how its other clinical and commercial Cell Shuttle programmes progress following the loss of BMS. | | Primary Source | Bristol Myers Squibb and Cellares statements reported by BioSpace | | Relevant Date | 26 August 2026 | Discover how nuaxia can support your next medical education initiative:
Bristol Myers Squibb has terminated its partnership with cell therapy startup Cellares to manufacture its blood cancer treatment Breyanzi. The pharmaceutical company determined that Cellares' Cell Shuttle manufacturing platform could not meet requirements for commercial-scale production of the CAR-T therapy. The decision highlights ongoing challenges in manufacturing CAR-T therapies, personalised cancer treatments that remain difficult and expensive to produce. Breyanzi, approved by the US FDA in 2021 for treating lymphoma and other blood cancers, generated $1.36 billion in sales in 2025. The companies signed a deal in 2024 worth up to $380 million, under which Bristol Myers reserved manufacturing capacity across the US, EU, and Japan. Cellares CEO Fabian Gerlinghaus disclosed the customer loss over the weekend, stating the company will resize its workforce.
Bristol Myers ends blood cancer drug deal with cell therapy maker Cellares. By Thomson Reuters Aug 25, 2026 | 12:58 PM Aug 25 (Reuters) - Bristol Myers Squibb has ended its partnership with cell therapy startup Cellares to expand the manufacturing of its personalized blood cancer therapy, a company spokesperson told Reuters on Tuesday. Bristol Myers determined that Cellares' cell therapy manufacturing platform, Cell Shuttle, could not meet the requirements to make its CAR-T therapy, Breyanzi, at commercial scale, the spokesperson said. Cellares did not immediately respond to a Reuters request for comment. The development underscores the challenges of manufacturing CAR-T therapies, a personalized form of cancer treatment that has transformed care for some blood cancer patients but remains difficult and expensive to produce. Breyanzi, first approved by the U.S. FDA in 2021, is used to treat lymphoma and other blood cancers. It generated $1.36 billion in sales in 2025. Endpoints News first reported the development earlier in the day. Cellares CEO Fabian Gerlinghaus had disclosed the loss of a "large pharmaceutical customer" in a LinkedIn post over the weekend, adding that this will force the company to "resize" its workforce. The start up did not immediately respond to a request for comment on the layoffs. The companies signed a deal in 2024 worth up to $380 million under which Bristol Myers reserved manufacturing capacity across the U.S., the European Union and Japan for CAR-T therapies. Bristol Myers' decision only applies to Breyanzi and its approved manufacturing process. CAR-T therapies work by removing a patient's immune cells, reprogramming them in a lab to fight cancer, and infusing them back into the body. (Reporting by Kamal Choudhury in Bengaluru; Editing by Sahal Muhammed)
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Industries
Company Size
201-500
Company Stage
Series D
Total Funding
$682M
Headquarters
South San Francisco, CA
Founded
2019
Find jobs on Simplify and start your career today
Don't see your dream role? Check out thousands of other roles on Simplify.Browse all jobs