With more than 300 trials in preclinical and clinical development actively using AAV as their vector of choice, the priority for any company working in this space is to ensure that each and every one of those therapies is the safest version it can be.
By addressing key topics including how to extract the most relevant data from preclinical studies to better inform how humans will respond to an AAV-based therapy in the clinic, analyzing potential integration risks of AAV serotypes, and investigating regulatory approaches to safety packages for submission, this meeting will inform how to streamline AAV safety processes to de-risk delays and shorten timelines to approval.
Join us in Boston to be part of the solution to bringing safer, effective genetic therapies to patients and gain immediately implementable insights to sharpen your programs currently in preclinical and clinical development.
To know more visit: https://ter.li/6gzgy4