AGENDA
Programme will be added once finalised.
Check the program of the previous edition HERE
DAY 1
Thursday, 22 May 2025
8h15
Welcome coffee and registration
8h45
Welcome address
- Plenary
Chairman

Charles Wolf
Country Lead Sanofi
Sanofi - France
9h00
Current Landscape and Pipeline Trends in Cell & Gene Therapy

Gavin Vuddamalay
Head of Scientific Affairs & Business Intelligence
MabDesign - France
9h15
Keynote lecture: Pioneering Research and Applications in iPS cells
- Plenary
Chairman
9h15
Organoids vs human pluripotent stem cells for cell based therapy


Ludovic Vallier
Einstein Professor for stem Cells in Regenerative Therapies
Berlin Institute of Health - Germany
9h45
Track 1: Pioneering Research and Applications in iPS cells
- Plenary
Chairman
9h45
Translation of pluripotent stem cell-based liver cell therapy into the clinic from an industrial perspective


Tuan Huy Nguyen
Co-Founder, President, and Chief Science Officer
GoLiver Therapeutics - France
10h05
Established new immunodeficient large animal model for receiving human induced pluripotent stem cell-derived hematopoietic grafts.


Mathias Brunet-Manquat
PhD Student
Etablissement Français du Sang / Centre de Recherche de Saint Antoine - France
10h25
Cross-Cutting Talk
- Plenary
Chairman
10h25
Liver-Directed Gene Therapy Using Immune-Shielded Lentiviral Vectors for Methylmalonic Acidemia


Julianne Smith
Chief Development Officer
Genespire - Italy
10h45
Coffee break - Exhibition Hall
11h15
Roundtable: Lessons Learned: Insights from Biotechs Post-Fundraising
- Plenary
Animated by MabDesign


Olivier Nègre
Chief Scientific Officer
Smart Immune, France


Philippe Chambon
Chairman, Ceo and founder
EG427, France


Rodolphe Clerval
CEO
Coave Therapeutics - France


Raphaëlle Kieffer
Head of Innovation Funding
MabDesign - France

Geoffrey Richard
Head of Private Finance
MabDesign - France
12h15
Lunch - Exhibition Hall - B2B Meetings
13h00
Roundtable: Rapid Sterility - Current Developments, Challenges and Emerging Perspectives
- Plenary
Animated by bioMérieux


Hélène Nègre
Pharmaceutical Affairs Director
CELLforCURE by Seqens, France


Guillaume Churlaud
Pharmacist, ATMP QC Manager
EFS, France


Marc Meichenin
chief scientific officer
Clean Cells, France


Caroline Kassim
R&D Biosciences Manager
bioMérieux, France


Guillaume Devun
Business Manager Rapid Methods
bioMérieux, France
14h00
Keynote lecture: Viral and Non-Viral Vectors : target optimization
- Plenary
Chairman
14h00
Development and validation of an intravenous AAV gene therapy for mucopolysaccharidosis type IIIB in mouse and dog model of the pathology


Francoise Piguet
Head of the innovation unit GENOV
Institut du Cerveau - France
14h30
Track 2: Viral and Non-Viral Vectors : target optimization
- Plenary
Chairman
14h30
Developping AAVs with improved safety and efficacy in neuromuscular disorders


Stephane Degove
CEO
Atamyo - France
14h50
Improving AAV Vectors efficacy and specificity via chemical conjugation


Lolita Petit
CSO
Coave Therapeutics - France
15h10
Development of targeted LNP

Catalina Bordeianu
Laboratory Head, Principal Scientist
Sanofi - France
15h30
Dynamic Carriers for RNA Delivery and Genome Editing


Ernst Wagner
Professor of Pharmaceutical Biotechnology
Ludwig-Maximilians-Universität (LMU) - Germany
Center of Nanoscience in Munich - Germany
15h50
Accelerating Non-Viral Delivery: From Custom Components to Scalable Manufacturing Solutions


Philippe Clavel
CEO
Curapath - Spain
16h10
Scaling Up Cell and Gene Therapy Biomanufacturing with high quality raw materials and dedicated solutions


Mourad Ferhat
Regional Director (France/BeneLux Region)
Acrobiosystems - Netherlands
16h20
Coffe Break - Exhibition Hall - B2B Meetings
17h00
Breakthrough innovation session
- Plenary
Chairman
17h00
Using mechanistic PK model to predict the human dose for AVM-022 gene therapy


Matthias Machacek
Managing Director
LYO-X - Switzerland
17h10
From design to clinic: Supporting advances in Cell and Gene Therapies through tailored plasmid manufacturing services


Nicolas Laugier
Sales
RD-Biotech - France
17h20
GREAT: Gene Recombination Along with Transposase


Francois Cherbonneau
CEO and Co-founder
QUIDDITAS - Belgium
17h30
Combination of TCR-deficient CAR-Tregs and non-mitogenic antiCD3 to promote transplant tolerance


Tifanie Blein
PhD Student
Institut Necker Enfants Malades - France
17h40
Tissue engineering based on human pluripotent stem cells for the treatment of Retinitis Pigmentosa and Age-related macular degeneration: a journey from preclinical to first clinical data


Karim Ben M’Barek
Research Scientist
I-Stem - France
17h50
Label free optical characterization of vector loading


Matthieu Greffet
President
UNVEIL - France
18h00
Innovative Human iPSC-Derived Retinal Organoid Model for AAV Gene Therapy Development


Amy Mawdesley
Business Development Manager
Newcells Biotech - United Kingdom
17h30
A Beating Cardiac Fibrosis on Chip Model to Predict the Efficacy of Drugs and Advanced Therapies


Erika Ferrari
Commercial Science Leader
BiomimX - Italy
18h30
Cocktail Reception hosted by Sanofi
- Plenary
19h45
End of day 1
DAY 2
Friday, 23 May 2025
8h30
Welcome coffee and registration
9h00
Track 3: Exploring the Future of CARs & TILs - session 1
- Plenary
Chairman
9h00
Nonclinical development of in vivo CAR-T for autoimmune diseases

Franck Chanut
Head of Preclinical Safety R&D Project France
Sanofi - France
9h20
The Dark Genome is a source of highly specific antigens for cancer immunotherapy


Michael Saitakis
Director, Immunotherapy
Mnemo Therapeutics - France
9h40
Alaya.bio: a polymeric gene delivery platform for in vivo CAR-T treatments


Renaud Vaillant
Founder and President
Alaya.bio - France
10h00
From Sequence to Cure: DNA/RNA Analytics in Cell and Gene Therapy


Sergey Yakushev
Head of Genetic Analysis
Microsynth - Switzerland
10h10
Coffee break - Exhibition Hall
11h00
Track 3: Exploring the Future of CARs & TILs - session 2
- Plenary
Chairman
11h00
Antigen selective CAR-T applied to autoimmune diseases


Christian Jorgensen
Director
IRMB - Institute for Regenerative Medicine & Biotherapy - France
11h20
Implementing co-creation with patients in the context of a Phase II pragmatic clinical trial to optimize treatment with TILs therapy


Emma Gillanders
Project Manager - Cancer Survivorship Group
Institut Gustave Roussy - France
11h40
How to address complexity? The point of view of the biomanufacturing partner


Célia Mercier
Business Developer EFS Bioproduction
EFS - France
12h10
Lunch - Exhibition Hall - B2B Meetings
Revolutionising Cell and Gene Therapy: Accelerating CAR T Processes and Drug Development
- Plenary
Chairman
13h00
24 Hour CAR T Process


Jerome Cabeau
Business Development Manager for Cell & Gene Therapy
Thermo Fisher Scientific - France
13h30
Accelerator Drug Development Initiatives


Pavithra Singaravelu
Senior Business Development Executive - Biotech Solutions
Thermo Fisher Scientific - France
14h00
Keynote lecture: Exploring the Future of CARs & TILs
- Plenary
Chairman
10h00
Title to be announced
14h00
A new class of tumor targets for next-generation cancer immunotherapies


Sebastian Amigorena
Team Leader
Institut Curie - France
14h30
Track 4: Gene Editing: Innovations, Challenges, and Applications
- Plenary
Chairman
14h30
The challenges of gentically modified Treg cell therapy in autoimmune disease and transplantation


Makoto Miyara
Professor
AP-HP, Assistance Publique - Hôpitaux de Paris - France
14h50
Advanced TALEN gene-editing for overcoming barriers to the success of CAR-T cells in solid tumors


Laurent Poirot
Senior Vice President, Immunology
Cellectis - France
15h10
POLYPRIME: a novel DNA Polymerase-based prime editing strategy


Jean-Paul Concordet
Researcher
Muséum National d'Histoire Naturelle - France
15h30