Biomanufacturing complexity, yield and cost have long constrained the promise of cell and gene therapies. In this webinar, featured speakers will explore the transformative potential of stable producer cell lines and how they’re poised to reshape CAR-T and viral vector production. These technologies once enabled monoclonal antibodies to evolve from niche laboratory tools into a $200 billion global market.
Webinar attendees will learn how many lessons from over 30 years of Chinese hamster ovary (CHO)-based antibody manufacturing can be applied to today’s CAR-T scale-out challenges. The speakers will also discuss why conventional transient transfection processes often struggle to keep pace with the escalating demand for next-generation therapies. They will unpack the quantitative advantages of stable versus transient methods through practical comparisons and illustrate how a novel platform addresses critical hurdles such as toxicity, low titers and regulatory consistency. Attendees will learn about the downstream benefits for cost reduction, timeline acceleration and broader patient access.
By reviewing data that demonstrate how core hurdles in stable cell line development have been overcome, attendees will gain valuable insights into overcoming common challenges. The webinar will also unveil a novel cell pool strategy designed to slash upfront time and investment, offering a data-driven roadmap for integrating stable cell line strategies into CMC workflows.
Whether a scientist optimizing bioprocesses, a CMC professional overseeing clinical manufacturing or a business leader charting commercialization strategy, this session will equip attendees with the insights needed to break the biomanufacturing bottleneck.
Register for this webinar to discover how stable cell lines can cut production costs, boost therapeutic yields and unlock truly scalable, GMP-compliant CAR-T biomanufacturing.
Speakers

Johanna Goldmann, Business Development Manager, ProBioGen
Johanna Goldmann is a Business Development Manager for viral vectors and cell and gene therapy at ProBioGen. Trained at the Scripps Research Institute, the Massachusetts Institute of Technology (MIT) and the Centre for Genome Regulation, she brings together cutting-edge science and commercial strategy. Johanna has authored numerous publications in leading journals and helped establish strategic partnerships to advance vector scale-up and support the adoption of next-generation therapies. Her expertise in translating complex research into scalable, GMP-compliant solutions strengthens ProBioGens position in CAR-T and viral vector manufacturing. Johanna’s commitment to innovation continues to contribute to the field of cell and gene therapy commercialization.

Sophia Sörensen, Research Scientist, ProBioGen
Sophia Sörensen is a Research Scientist with over 12 years of experience at ProBioGen, currently working in the Viral Vectors and Gene Therapeutics department. She holds an MSc in Biotechnology from the Berlin University of Applied Sciences. Sophia began her career in cell line development for protein-based biologics, focusing on the generation of high-producing cell lines for CHO-based antibody production. She later transitioned to viral vectors, playing a key role in developing stable lentiviral packaging and producer cell lines. Her contributions were instrumental in establishing Lenti.RiGHT®, ProBioGen’s scalable lentiviral vector platform. Today, she and her team drive innovations in vector yield and scalability — across both lentiviral and AAV systems — through strategic cell line optimization and advanced process development.
Who Should Attend?
This webinar is ideal for the following:
- Cell and gene therapy scientists and researchers
- CMC and bioprocess development professionals
- Manufacturing and operations managers in biotech
- Business executives and strategic stakeholders in cell and gene therapy
What You Will Learn
Attendees will learn:
- How a 30-year track record of CHO-based antibody biomanufacturing informs today’s viral vector challenges
- Why traditional transient transfection processes hit a cost and scale ceiling for CAR-T
- The numbers behind it all: cost-per-dose and consistency improvements offered by stable producer cell lines
- ProBioGen’s Lenti.RiGHT® platform features and its impact on scalable, GMP-compliant CAR-T manufacturing
Xtalks Partner
ProBioGen
ProBioGen is a fully integrated contract development and manufacturing organization (CDMO) specializing in biopharmaceuticals, viral vectors, and vaccines. We offer high-performance cell line development, robust process optimization, reliable GMP manufacturing, and advanced analytical services. Leveraging proprietary technologies, we deliver high yields while ensuring exceptional potency and quality, while our expertise spans therapeutic proteins, viral vaccines, and cell and gene therapies. As a trusted partner, ProBioGen provides tailored, scalable solutions that address complex development and manufacturing challenges—from early-stage programs to GMP production.
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