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International Society Cell & Gene Therapy 2023

International Society Cell & Gene Therapy 2023

Date: May 31-June 3, 2023

Location: Palais des Congrès de Paris 


Event Website: https://www.isctglobal.org/isct2023/home

 

MEET OUR TEAM AND LEARN ABOUT AGC BIOLOGICS

Interested in learning more about our global network and capabilities? Click the button below or email our attending representative at the event to set up a meeting.

Click the link above to get all the details. 

REQUEST A MEETING

You can also reach out directly to our expert attending the show

Manuel Balbuena
Business Development Director
Email  me

Introducing our new AAV & LVV Platforms

End-to-end viral vector offerings give developers plug-and-play templates for the entire development and manufacturing process

Our new templated adeno-associated viral vector platform.

 Learn about Bravo

Our new templated lentiviral vector platform.
 

Learn about our cell and gene therapy services 

Cell Therapy Production and Manufacturing

AGC Biologics’ cell therapy services support every stage of the product journey, from pre-clinical through commercialization. At our Milan and Longmont facilities, we can work with virtually any cell type – including Human Mesenchymal Stem Cells (hMSCs), Exosomes, CD34+, T-Cells, NK Cells, and more.  

Using the latest autologous and allogeneic methods, we help your products meet the exact specifications for patients in a clinical or commercial setting. 

Learn more about our overall cell therapy offering 

 

Plasmid DNA (pDNA) Materials 

To support your pDNA needs, AGC Biologics utilizes a customized process based on your specific plasmid and hosting system. We have extensive technical expertise in fermentation, purification, and analytics, and our highly experienced teams routinely manufacture GMP-grade pDNA materials. This work includes starting material for gene therapy, and viral vector manufacturing. 

Learn more about our Plasmid offering

 

Viral Vector Production and Manufacturing 

AGC Biologics scientists have two decades of viral vector-based gene therapy expertise and specialize in adeno-associated viral vectors (AAV), lentiviral vectors (LVV), and retroviral vectors (RVV). Our sites in the U.S. and Italy have supported four commercial products. 

Our ready-to-use platform capabilities for AAV and LVV programs are built on cell factories and bioreactors using adherent and suspension processes, designed entirely in-house. 

Discover more about our viral vector services 

 

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