Viral vectors are currently the preferred gene-delivery vehicle for most cell and gene therapies and clinical trials require high titer virus preparations to adequately deliver the therapeutic transgenes to clinical subjects or target cells. For this reason, technologies that enable the industrialization of these processes in a safe, robust, and cost-effective way are necessary to support the demands of the patient population. However, complexity around developing and scaling viral vector processes to commercial manufacturing scale, and the lack of standardized approaches remain as challenges that can impact therapy development timelines and productivity. Selection of the appropriate production platform plays a key role on the successful implementation of a process that meets the commercialization timelines and manufacturing costs. We will share a case study that demonstrates the successful steps taken to develop and scale up a customer process for a Helper-Dependent-Adenovirus (HDAd), leveraging Pall’s process expertise, and the iCELLis® bioreactor platform, to help accelerate the development timelines. Critical process parameters for development and manufacturing, such as seeding density, infection density, and harvest strategy, were first tested at the flatware stage, and continually optimized over the course of the iCELLis Nano development stage. The optimized parameters were used successfully in duplicate scale-up batches at the iCELLis 500+ scale to demonstrate a process ready for transfer to a clinical manufacturing facility.
Learning Objectives:
Define steps needed to scale-up an adherent production process for gene therapy
List key parameters for process development in a fixed-bed bioreactor
Understand scale-up considerations when going from flatware to large scale bioreactors