The challenge of scalable AAV manufacture for
gene therapies, and how to overcome it.
Gene therapies offer enormous promise for the treatment of genetic disease. There
are over 1,000 cell and gene therapy clinical trials underway worldwide, indicating
the great potential of this new class of medicines. However, large-scale
manufacture of the viral vectors required to deliver therapeutic genes into patients
still represents a stumbling block in the path to market for gene therapies...
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