Overcoming Regulatory, Safety/Efficacy, And Toxicity Hurdles

What are the biggest challenges the mRNA/RNA therapeutics field is struggling with in development today — and are we focused on solving the right challenges?  

The rapid development, scale-up, and successful commercialization of mRNA vaccines served as a great case study on the important role mRNA/RNA therapeutics can play in society. However, for those striving to develop next-gen RNA therapeutics, achieving more specifically targeted non-viral delivery is a large hurdle to broadening these therapeutics’ applicability, durability, and effectiveness.

On October 4, 2022 Bioprocess Online Live hosted a panel discussion digging into the scientific-, development-, and business-related advancements that will enable the RNA therapeutics industry to meet the needs of a broader array of patient populations.

In this segment, Russell Johnson, VP Formulation Research for RVAC Medicines, and Aalok Shah, Director of Formulation & Drug Delivery, Strand Therapeutics, discuss what industry challenges should be top of mind for experts as it relates to the regulatory paradigm, toxicity/safety, and in vivo modeling.

View the full presentation on-demand here.