CDMO VIVEbiotech Expanding Facilities To Increase Manufacturing Capabilities For Lentiviral Vectors

• VIVEbiotech expands facilities to increase innovation and manufacturing capabilities of specialist lentiviral vectors
• New facility provides additional clean rooms to cater for increase in lentiviral demand from gene and cell therapy sectors

VIVEbiotech, S.L., a gene transfer technologies Contract Development and Manufacturing Organization (CDMO) developing and GMP manufacturing lentiviral vectors, today announces it is expanding its manufacturing capabilities with new facilities.

The expansion of VIVEbiotech facilities will enable increased production capacity and the further optimization of its manufacturing processes. Versatility in the design will result in a more flexible configuration enabling the possibility of further clean rooms in the future as well as making it feasible accommodating a much larger number of batches.

In addition, the expansion will provide the additional space for VIVEbiotech to invest in additional manufacturing capital and equipment to be able to respond to the different phases of upcoming projects. This will also cater for the international market requirement for an increase in sophistication of lentiviral manufacturing, with a combination of flexibility, cost-effectiveness and an increase in efficiency.

“The continued expansion of the gene and cell therapy sector has resulted in an increase in the number of clinical trials, as well as additional trials moving into later-stage development. In turn, this has led to a continued increase in the demand for both lentiviral vectors, as well as expertise in their use and application,” said Gurutz Linazasoro, CEO of VIVEbiotech S.L. “This demand for lentivirals is increasing for therapies throughout the clinical stages and into commercialization. A higher number of early-stage cell and gene therapy developers now are requiring a longer-term partner in lentiviral supply that provides continuity throughout the clinical stages. VIVEbiotech has responded to this growth in requirement from the cell and gene therapy sector by constructing new facilities with increased cleanrooms to cater for the demand, and a renewed focus on innovation to continue leading the development of lentiviral vectors. This will enable us to utilize our sole lentiviral expertise and specialization to contribute towards moving gene therapies through the clinical process and to patients in a range of different conditions.”

The new facilities will also provide the potential for VIVEbiotech to further advance the optimization of lentiviral-vector properties and the associated manufacturing process. Therefore, VIVEbiotech has a highly qualified team specialized both in manufacturing and in virology. This is required as the international gene and cell therapy sectors move into a broader spread of indications that affect more patients and use more innovative applications.

The new facilities are expected to be completed in April 2021, and VIVEbiotech aims for the transition between the facilities to be completed in October.

About VIVEbiotech S.L.
VIVEbiotech is a company fully specialized in lentiviral vectors with expertise as a GMP CDMO focused on the manufacture of lentiviral vectors from R&D early stages to GMP. Working with European, US, Australian and Asian companies, its main aim is to adapt to customer own requirements with high flexibility from a technical and timeline perspective. In addition, VIVEbiotech´s technology development strategy is focused on providing a response to the main hurdles that currently exist within the gene therapy field, mainly the need of cost-effective and regulatory compliant processes, and the enhancement of the safety profile of viral vectors. For more information, visit https://www.vivebiotech.com/