Cell and Gene Therapy at SIRION
We specialize in designing and engineering viral vectors to support development of the safest, most cost effective, and most efficacious cell and gene therapies. We perform active R&D in the areas of AAV and lentiviral vector optimization focused on vector design for clinical use, plus upstream and downstream process development to enhance productivity and reduce manufacturing contaminants.
Our portfolio includes technologies to optimize capsid specificity and targeting, high-throughput lead vector identification, targeting of therapeutic genes, and gold standard transduction technologies.
SIRION technologies are currently used in over 50 clinical programs ranging from phase 1 to 3, in the USA and Europe, plus one approved therapy.
Cell and Gene Therapy Support
Our experienced cell and gene therapy professionals can guide you through our capabilities, and work closely with you to manage your project for optimum results.
They will work with you on:
Providing an overview of all SIRION technologies which could support your project
In-depth analysis and consulting of CGT projects for improved efficacy and patient safety
Development of viral vector designs optimized for clinical applications
Therapeutic expression cassette optimization for efficacious and safe expression profile
Process development for optimal manufacturing productivity and negligible impurity levels
PoC and biodistribution studies of the lead candidate batches in large animals with a CRO network
Find out more about how SIRION can help cell and gene therapy developers to accelerate the development of R&D and preclinical programs for AAV Vectors for Gene Therapy and Lentiviral Vectors for Cell Therapy.