In the rapidly advancing field of cell and gene therapy, manufacturing recombinant AAV therapeutics has remained inefficient. Older legacy processes often yielded only a handful of doses for patient treatment, underscoring the need for more efficient manufacturing methods. Today, AAV therapies necessitate high titers and high-quality viral genomes per dose, making optimizing AAV production processes critical to reducing overall costs and improving accessibility. This challenge limits scalability, driving up the costs of these therapies.
In this webinar, we will discuss AAV production challenges and the strategies, workflows, and technologies employed to overcome them. In collaboration with partners, improvements as a result of next generation AAV production technologies, lead to fold increases in the number of therapeutic doses produced per bioreactor and reduces costs per AAV dose. Further, our experts will delve into technical solutions, sharing their insights on how to achieve these fold increases and cost reductions in cell and gene therapy applications.
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