Los Angeles Convention Center
Los Angeles, CA
May 16-20, 2023

Catalent Cell & Gene Therapy



We look forward in meeting you. Come and meet the team.

Catalent Cell & Gene Therapy is a full-service partner for adeno-associated virus (AAV) vectors and CAR-T immunotherapies, with deep experience in viral vector scale-up and production. Catalent has a global network of clinical and commercial manufacturing facilities, and fill-finish and packaging capabilities located in both the U.S. and Europe. Catalent Cell & Gene Therapy has produced more than 100 cGMP batches across 70+ clinical and commercial programs.


 Products

  • UpTempo Virtuoso™ AAV Platform Process
    Catalent’s UpTempo Virtuoso™ AAV platform process is a scalable, CGMP-ready process for viral vector manufacturing that can reduce the current 18-20-month development timeline for drug product in half....

  • As the pipeline of viral vector-based therapies continues to reach later stage studies, a standardized manufacturing process is necessary for chemistry, manufacturing and control (CMC) requirements from regulatory agencies and to meet the accelerated timelines for first-in-human studies of advanced therapeutics. Catalent’s UpTempo Virtuoso™ AAV platform process is a scalable, CGMP-ready process for viral vector manufacturing that can reduce the current 18-20-month development timeline for drug product in half.

    The platform process was developed for standard AAV serotypes, including 1, 2, 5, 6, 8, and 9. With the completion of reference standard and toxicology batches, the upstream and downstream processes are locked for CGMP production at up to 400L scale. Overall, starting with CGMP grade plasmid DNA and a master cell bank, with the UpTempo Virtuoso™ platform, the development and manufacturing process will yield drug product in 9 months. Catalent’s platform process partners will also have access to our integrated supply chain of plasmid DNA, potentially further streamlining their timeline.