SK pharmteco’s subsidiary Yposkesi launches AAVelocity, a plug-and-play Adeno-Associated Virus (AAV) platform
Designed to shorten turnaround on manufacturing AAVs, this new platform offers Cell and Gene Therapy developers more flexibility in producing viral vectors for clinical and commercial use
Yposkesi, SK pharmteco’s European clinical and commercial viral vector manufacturing subsidiary for Cell and Gene Therapies (C>), today launches AAVelocityTM, a plug-and-play Adeno-Associated Virus (AAV) platform. AAVelocity is designed to bring cost and time efficiencies to drug developers in the production of AAV gene delivery systems used to transport gene therapy into tissue to prevent, treat, or cure inherited disorders and rare diseases.
The AAVelocity plug-and-play platform can provide a 12-month turnaround on drug developer projects, lowering industry average standard bioprocessing timeframes by at least six months and helping clients save on associated costs.
Also new is AAVelocity’s inherent flexibility. This enables bioproduction teams to easily adapt to client requirements, such as achieving different purity levels within strict time constraints. It includes delivering AAVs containing the optimized amount of genetic material.
AAVelocity’s agility also avoids intermediary steps or the addition of others while ensuring total integrity and purity of the genetic material. The improved efficacy of AAVelocity will bring greater benefits to drug developers and their pipelines, according to SK pharmteco. Using single-use bioreactors, the AAV platform is scalable to meet any client need: 10L > 50L > 200L > 2 x 200L > 1000L.
“SK pharmteco, through Yposkesi, is pleased to launch a second platform for viral vector manufacturing with enhanced plug-and-play capabilities. Leveraging Yposkesi’s many years of expertise, SK pharmteco is able to offer a genuine cost and time-effective solution for AAV manufacturing to stay in step with the increasing development and approvals of C> treatments we are witnessing today, which are set to evolve in the near future,” said Alain Lamproye, Yposkesi division head. “AAVelocity will bring tangible benefits to the C> market: high yields, scalability, robustness, consistency, and flexibility like no other. Clients can also benefit considerably from Yposkesi’s strong track record in AAV manufacturing and its experience of participating in filing six IND1/IMPD of AAV-based products since 2017.”
The strengthening of AAV manufacturing at its subsidiary aligns with SK pharmteco’s positioning to meet the growing demand.
According to the Nice Insight report ‘Cell and Gene Therapy: 2023 Market Analysis, CDMO Pricing, and Benchmarking’: “AAV-based therapies are set for greater approval number and approval of treatments for more prevalent diseases,” making it the most represented viral vector within those therapies starting in 2025. By 2028: “Sales of AAV-associated cell and gene therapies are projected to be 72% higher than LV-based therapies.”
AAVelocity key features:
- -High yields: 3×1010 VG/mL up to 2×1011 VG/mL
- -Scalable from 250ml for R&D, up to 1,000L for cGMP batches
- -Robustness: No loss of titer when scaling up
- -Enriched: >80% full particles
Further capabilities, including plasmid manufacturing, process development, GMP vector manufacturing suites, integrated testing & analytics, regulatory services, and an adherent AAV manufacturing platform, are available at the Center for Breakthrough Medicines (CBM), SK pharmteco’s US clinical and commercial viral vector manufacturing subsidiary for C>.
1 Investigational New Drug/Investigational Medicinal Product Dossier
Yposkesi is SK pharmteco’s European clinical and commercial viral vector manufacturing subsidiary for Cell and Gene Therapies (C>). Located in the south of Paris, France, Yposkesi is one of Europe’s largest CDMOs for viral vector manufacturing in Cell and Gene Therapies.
Now unified with the Center for Breakthrough Medicines (CBM) in the Philadelphia region, USA, Yposkesi and CBM offer a full range of services throughout the entire advanced therapy process, from research and development to manufacturing and commercialization. With locations in Europe and the US, together they operate multiple manufacturing suites for bulk drug substances and fill and finish to support the growing demand for late-phase projects.
About Center for Breakthrough Medicines
Center for Breakthrough Medicines (CBM) is a purpose-built and patient-driven, cell and gene therapy contract development and manufacturing organization (CDMO) uniquely positioned to enable pharma and biotech companies to develop, test, and manufacture life-saving therapies on a global scale. Ideally located in the heart of Philadelphia’s Cellicon Valley, CBM is the U.S. headquarters for SK pharmteco Cell & Gene, which is comprised of CBM and Paris-based Yposkesi, a viral vector CDMO, who together have assembled the most accomplished experts in the world, armed with cutting-edge and innovative technologies, to offer scalable, end-to-end, best-in-class services to provide life-changing – and life-saving – therapies around the world.
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