Business Wire

TreeFrog Publishes Results of First Successful Bioproduction of a Parkinson’s Disease Cell Therapy in Scalable Bioreactor in Neurotherapeutics Journal

Share

Publication demonstrates the cell therapy product for Parkinson’s Disease overcomes most complex challenges in bioproduction, while demonstrating full behavioral recovery in pre-clinical model

TreeFrog Therapeutics, a regenerative medicine biotech focused on using its proprietary GMP compliant technology platform, C-Stem™, to develop life-saving cell therapies, today published an article in Neurotherapeutics, demonstrating the first successful bioproduction of a Parkinson’s Disease cell therapy in a scalable bioreactor, leading to full behavioral recovery 16 weeks after transplantation using a cryopreserved 3D microtissue format.

This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20241009598667/en/

TreeFrog Therapeutics 10L bioreactor for cell therapy (Photo credits: TreeFrog Therapeutics)

The potential of cell therapy for Parkinson’s Disease is well documented – dating back to pioneering studies in the 1980s using fetal cell transplants – and scientific progress over the last decades provides great hope for the future. The emergence of induced pluripotent cells (iPSCs) opened new pathways and solved one of the first major challenges, cell sourcing. However, multiple hurdles remain, particularly around industrialization and no cell therapy for Parkinson’s Disease has advanced beyond clinical stage to date.

“Today’s publication demonstrates how TreeFrog Therapeutics has overcome the most complex challenges of developing a successful treatment for Parkinson’s disease using our C-Stem™ platform technology and producing a therapy containing mature dopaminergic neurons with a unique 3D format that promotes cell survival post-graft with proven pre-clinical results. We are excited to present the paper to the scientific community and look forward to many discussions on our scientific and bioproduction progress. I am proud of all the work done by Nicolas Prudon, lead author, alongside colleagues at TreeFrog”. Jens Schroeder, Chief Medical Officer, TreeFrog Therapeutics.

The paper published online today reinforces the potential of TreeFrog’s cell therapy to overcome several complex challenges, one of which being the limitation of the format. Most other existing investigational cell therapies use single-cell suspensions which have an elevated risk of inducing cell death through anoikis affecting survival and/or potency of the product post-transplantation1. The results achieved with the unique 3D format of TreeFrog’s cell therapy product demonstrate the potential to circumvent this limitation, providing protection to the more mature, sensitive cells that are neurons.

Another challenge facing companies is the bioproduction strategy. While currently only scale-out methods have been employed, which increase the potential of variability due to the manually intensive methods required, C-Stem™ production use a scale-up strategy with a stirred-tank bioreactor enhancing productivity and reducing costs. The system is commercial scale ready for the Parkinson’s disease cell therapy, with doses for hundreds of patients in one 10L bioreactor.

Finally, as in downstream processing, cryopreservation has proven to be a major challenge in the cell therapy space with fresh product performing better, while cryopreserved product resulted in a delayed time-to-effect.2 The results published today, demonstrate the same efficacy with the cryopreserved product, as the fresh product, with no time-to-effect delay.

Detailed analyses and discussion of the bioproduction process, product characterization and pre-clinical efficacy results can be found in the full paper, available here.

-Ends-

About Parkinson’s Disease
Parkinson’s Disease is a progressive neurological disease affecting more than 10 million people worldwide3 with prevalence doubling in the last 25 years.4 The complex disease is the result of the degeneration of specific dopamine-producing neurons in the brain. There is a huge unmet need as current treatments provide symptomatic relief only and medication fails to control symptoms for nearly 75% of people.5 Regenerative medicine and in particular, cell therapy, holds great potential as it can replace these lost neurons, ultimately restoring function.

About C-Stem
The proprietary biomimetic C-Stem™ technology platform is based on a decade of research bringing together stem cell biology, biophysics and bioproduction. It is the world’s first GMP compliant cell encapsulation device capable of generating over 1,000 capsules per second, enabling the seeding of bioreactors up to 10 liters and delivering 15 billion iPSC cells in a single batch.

Blending microfluidics and stem cell biology, the C-Stem™ technology generates alginate capsules seeded with induced pluripotent stem cells (iPSCs) at very high speed. Engineered to mimic the in vivo stem cell niche, the capsules allow iPSCs to grow exponentially in 3D, and to differentiate into ready-to-transplant functional microtissues. The alginate is both porous and highly resistant, allowing the encapsulated iPSCs to expand and differentiate in large-scale bioreactors without suffering from impeller-induced shear stress. The breakthrough technology addresses critical challenges in the industry of scale and quality, in addition to the efficacy and safety of future cell therapy products.

About TreeFrog Therapeutics
TreeFrog Therapeutics is a French-based biotech company set to unlock access to cell therapies for millions of patients. TreeFrog is unique in its approach to cell therapy development bringing together biophysicists, cell biologists and bioproduction engineers to address the challenges of the industry — producing and differentiating cells of quality at unprecedented scale, cost-effectively. To realize their mission of Cell Therapy for all, TreeFrog operates a business model that includes its own therapeutic programs and partnerships with leading biotech and industry players in other areas. In the last 3 years, the company has raised $82 million to advance a pipeline of stem cell-based therapies in regenerative medicine. In 2022, the company opened technological hubs in Boston, USA, and Kobe, Japan, to drive the adoption of the C-StemTM platform and establish strategic alliances with leading academic, biotech and industry players.

www.treefrog.fr

1 Gilmore A.P., Anoikis, Cell Death Differ, 12 (2005), pp. 1473-1477
2
Hiramatsu S., Morizane A., Kikuchi T., Doi D., Yoshida K., Takahashi J., Cryopreservation of induced pluripotent stem cell-derived dopaminergic neurospheres for clinical application, J Park Dis., 12 (2022), pp. 871-884
3
Statistics | Parkinson's Foundation
4Parkinson disease (who.int)
5www.parkinsons.org.uk

View source version on businesswire.com: https://www.businesswire.com/news/home/20241009598667/en/

Subscribe to releases from Business Wire

Subscribe to all the latest releases from Business Wire by registering your e-mail address below. You can unsubscribe at any time.

Latest releases from Business Wire

Phase 3 Data for Incyte’s Retifanlimab (Zynyz®) in Patients with Squamous Cell Carcinoma of the Anal Canal (SCAC) Published in The Lancet13.6.2025 00:45:00 CEST | Press release

POD1UM-303/InterAACT 2 is the first and largest global Phase 3 trial evaluating a PD-1 inhibitor in combination with chemotherapy for the treatment of patients with advanced SCAC not previously treated with systemic chemotherapy The trial met its primary endpoint; treatment with retifanlimab in combination with platinum-based chemotherapy (carboplatin-paclitaxel) resulted in clinically meaningful improvements in progression-free survival and overall survival In May 2025, the U.S. Food and Drug Administration (FDA) approved Zynyz® (retifanlimab-dlwr) in combination with carboplatin and paclitaxel and as a single agent for the treatment of advanced SCAC; submissions to other global regulatory agencies are also under review Incyte (Nasdaq:INCY) today announced that primary results from the Phase 3 POD1UM-303/InterAACT 2 trial of retifanlimab (Zynyz®), a humanized monoclonal antibody targeting programmed death receptor-1 (PD-1), in combination with carboplatin and paclitaxel (platinum-base

Güntner Drives Group-Wide Innovation in 2024 Sustainability Report12.6.2025 21:30:00 CEST | Press release

Progress in natural refrigerants, water efficiency and circular economy underscores Güntner’s global impact Güntner, a global leader in refrigeration and heat exchange technology, today announced its featured role in the newly released 2024 A-HEAT Sustainability Report. The report outlines significant progress toward ambitious environmental goals—fueled by Güntner’s commitment to measurable, innovation-led sustainability. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20250612897493/en/ Güntner advances global sustainability goals with progress in natural refrigerants, water savings, and circular economy efforts. Working toward its 2030 sustainability targets, Güntner delivered significant achievements across key areas including natural refrigeration integration, water and energy efficiency and the development of circular economy solutions. These efforts reflect Güntner’s ongoing mission to make sustainability not just a goal,

Windsurf Launches First GPU Cluster in Germany, Expanding Secure Enterprise AI in Europe12.6.2025 20:45:00 CEST | Press release

Windsurf launches a GPU cluster in Germany, delivering 50% faster performance and secure access to European enterprises. Data residency ensures enterprise repositories stay within the EU, meeting stringent security requirements. Windsurf already supports 100+ European enterprise customers, highlighting strong demand for AI-powered development tools across EMEA. Windsurf, a leader in AI-powered software development, today announced its first GPU cluster in Germany, as product demand surges and the company expands performance capacity across the EU. With over 100 local enterprise customers already using Windsurf products, the new cluster marks the company’s first major international step in building scalable infrastructure for the European market. Located in Frankfurt, home to some of the world’s strictest data security laws, the cluster was a natural choice for Windsurf’s first deployment. This cluster was specifically designed to meet the unique security and performance requirements of

Xsolla Partners With Defold to Enable Seamless In-game Purchases for Web Developers12.6.2025 19:00:00 CEST | Press release

New SDK Integration Simplifies Monetization for Defold Developers Publishing on CrazyGames Ahead of Global Game Jam Xsolla, a leading global video game commerce company, announces a new strategic partnership with Defold, the cross-platform game engine trusted by professionals and indie developers worldwide. This collaboration introduces a seamless integration between Xsolla and Defold-built web games on CrazyGames, enabling developers to easily monetize their titles just in time for the CrazyGames x Defold Game Jam running June 13–15. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20250612569206/en/ (Graphic: Xsolla) To address the complexity of in-game monetization, Xsolla and Defold have developed a new SDK that allows Defold developers to implement in-game purchasing functionality without the complex manual API setup required. With Xsolla’s sponsorship and support, this integration removes friction from the monetization jou

Pioneering Cancer Plasticity Atlas will Help Predict Response to Cancer Therapies12.6.2025 17:00:00 CEST | Press release

The Wellcome Sanger Institute, Parse Biosciences, and the Computational Health Center at Helmholtz Munich today announced a collaboration to build the foundation of a single cell atlas, focused on understanding and elucidating cancer plasticity in response to therapies. The collaboration will catalyze an ambitious future phase to develop a cancer plasticity atlas encompassing hundreds of millions of cells. Utilizing novel organoid perturbation and Artificial Intelligence (AI) platforms, the aim is to create a comprehensive dataset to fuel foundational drug discovery models and cancer research. Dr. Mathew Garnett, Group Leader at the Sanger Institute, and Prof. Fabian Theis, Director of the Computational Health Center at Helmholtz Munich and Associate Faculty at the Sanger Institute, will be the principal investigators in the collaboration. Garnett’s research team has generated novel 3D organoid cultures that serve as highly scalable and functional cancer models with the ability to capt

In our pressroom you can read all our latest releases, find our press contacts, images, documents and other relevant information about us.

Visit our pressroom
World GlobeA line styled icon from Orion Icon Library.HiddenA line styled icon from Orion Icon Library.Eye