Cell and gene therapy at Festival of Biologics 2026
Oct 13–15, 2026 Basel, Switzerland ~3k attendees Website
28 organizations at Festival of Biologics 2026 present work in cell & gene therapy: 12 suppliers and service providers, 9 academic, government and non-profit bodies and 7 drug developers. Between them they bring 88 presentations to the program. Most represented: Novartis (29 on the program), Roche (17 on the program), Lonza (6 on the program). 22 of them have their own page in this guide. As of Sep 26, 2026.
Format
Top represented
Showing 1–3 of 28 organizations
| Organization | Festival of Biologics 2026 Attendance |
|---|---|
Novartis Basel, Switzerland | |
Global pharmaceutical company whose contract manufacturing arm offers CDMO services for biologics, small molecules, cell and gene therapy, and fill-finish. | Booth Exhibiting at Booth 185 Keynote Tue Oct 13 09:10 Biotechnology, the Renaissance How advances in biology, AI and new treatment types are converging to change what medicine can do for patients. Chair Tue Oct 13 11:25 Chair Tue Oct 13 11:25 Chair Tue Oct 13 11:25 Talk Tue Oct 13 11:30 Panel Tue Oct 13 12:20 Chair Tue Oct 13 14:05 Talk Tue Oct 13 14:50 Intensified Upstream Processing: Fed‑Batch and Perfusion Options for Robust Scale-Up Ways to get more protein from cell cultures by feeding them steadily or continuously, and how to scale that up reliably. Talk Tue Oct 13 15:10 Panel Tue Oct 13 15:10 Panel Discussion: From Research to GMP: Making MSC Manufacturing Reproducible at Scale How to grow mesenchymal stromal cells, a kind of stem cell, the same way batch after batch as production scales up. Talk Tue Oct 13 15:30 Chair Tue Oct 13 16:45 Panel Tue Oct 13 17:30 Panel Discussion: Next Generation Antibody Formats Where antibody drug design is heading, from two-target antibodies and antibody-drug conjugates to AI's role in engineering them. Talk Tue Oct 13 17:30 What AI can do – or not – in Patient Engagement What AI can and cannot do when drug developers involve patients in research, and how to measure whether that involvement helps. Chair Wed Oct 14 11:25 Chair Wed Oct 14 11:25 Talk Wed Oct 14 12:10 Talk Wed Oct 14 12:30 Bovine AAV – a promising vector for pulmonary gene therapy Early results from using a cattle adeno-associated virus to deliver gene therapy to the lungs, including how immune systems recognise it. Talk Wed Oct 14 12:30 Chair Wed Oct 14 14:05 Talk Wed Oct 14 14:30 Commercial Considerations for CAR-T Therapy: Lessons Learned from Recent Blockbusters What makes CAR-T cancer therapies hard to sell worldwide, from complex manufacturing and shipping to getting treatment centres and payers ready. Talk Wed Oct 14 15:30 When the Target Moves: Building Robust DSP Through Science, Monitoring, and Learning Why purification steps that once worked can start failing when the material feeding them changes, and how monitoring catches that early. Chair Wed Oct 14 16:45 Chair Wed Oct 14 16:45 Talk Wed Oct 14 16:50 Talk Wed Oct 14 17:30 Protein Quality as a Critical Factor in Target Interference Assessment for Bioanalytical Assays How the quality of a lab-made protein can distort tests that check whether patients make antibodies against a biologic drug. Talk Wed Oct 14 17:50 An Oligonucleotide Program in Late-Stage Clinical Trials Lessons from keeping an anti-drug antibody test working for a cholesterol-lowering siRNA drug through late trials and a handover to a partner lab. Keynote Thu Oct 15 09:05 From Strategy to Delivery: Aligning Bioanalytical Innovation and Execution Across Clinical Phases How to decide what to measure, when and why, as biologic drugs move from early studies into late-stage clinical trials. Talk Thu Oct 15 09:40 Chair Thu Oct 15 11:15 Chair Thu Oct 15 11:15 |
Roche Basel, Switzerland | |
Swiss pharmaceutical and diagnostics company with a large biologics portfolio. | Chair Tue Oct 13 14:05 Talk Tue Oct 13 14:10 Talk Tue Oct 13 14:30 Novel Orthogonal Receptor Platform Activating the IL12 Pathway in CAR-T Cells Using a Small-Molecule Ligand An engineered receptor that lets a small molecule switch on interleukin-12 signalling in CAR-T cells, improving tumour killing in animal models. Talk Tue Oct 13 15:10 Chair Tue Oct 13 16:45 Talk Tue Oct 13 17:50 Chair Wed Oct 14 11:25 Talk Wed Oct 14 11:30 Strategy for potency determination of gene therapy products illustrated by rAAV Ways to measure whether a gene therapy made from adeno-associated virus actually works, and when an infectivity test can be skipped. Talk Wed Oct 14 14:30 Regulatory Reliance as a Catalyst for Biologics Access in Emerging Markets How regulators in emerging markets can lean on reviews already done by established agencies so patients get biologic drugs sooner. Talk Wed Oct 14 14:50 Talk Wed Oct 14 17:50 Chair Thu Oct 15 11:15 Talk Thu Oct 15 11:20 Talk Thu Oct 15 12:00 Emerging Immunogenicity Challenges for Next-Generation Biotherapeutics Why newer antibody drugs can trigger unwanted immune reactions that sequence checks miss, and what laboratory and animal data reveal about the causes. Talk Thu Oct 15 12:20 |
Lonza Basel, Switzerland | |
Contract development and manufacturing partner for biologics, cell and gene therapies and small molecules. | Booth Exhibiting at Booth 450 Talk Tue Oct 13 17:10 De-risking Lyophilization Scale-Up Using predictive models How computer models of freeze-drying can predict what happens at full manufacturing scale, cutting experiments and the risk of a failed transfer. Keynote Wed Oct 14 09:55 From Experimentation to Prediction: How Data-Driven Innovation is Forging Predictability Across Biologics Development and Precision Biomanufacturing Why biologics developers still decide by trial and error, and how treating every program as shared learning could make outcomes more predictable. Bioprocessing & manufacturingAI & computational design Talk Wed Oct 14 12:30 Accelerating CHO Cell Line Development Through Next-Generation Expression System Design How improved cell engineering, promoter design and selection methods shorten the path from DNA to a cell line that makes a drug. Talk Wed Oct 14 14:30 Beyond mAbs: accelerated Gene-to-IND development for bispecifics, Fc-fusions and high-concentration biologics Faster routes from DNA to first clinical trials for complex antibody drugs, and the problems they create in making, purifying and formulating them. |
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Browse Festival of Biologics 2026 by
Organization type
Topic
- Antibody & protein engineering 67
- AI & computational design 38
- Bispecifics & multispecifics 13
- ADCs & armed antibodies 18
- Immunotherapy & oncology 44
- Cell & gene therapy 28
- Therapeutic vaccines 13
- Peptides & GLP-1 7
- Bioprocessing & manufacturing 87
- CMC, formulation & analytics 58
- Clinical development 45
- Regulation & market access 40
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