AavantiBio Furthers Strategic Partnership With University of Florida To Research and Develop Next Generation Gene Therapy Capsids (Business Wire)

AavantiBio Furthers Strategic Partnership With University of Florida To Research and Develop Next Generation Gene Therapy Capsids

UF startup and UF Innovate | Accelerate company AavantiBio, a gene therapy company focused on transforming the lives of patients with rare genetic diseases, announced it is partnering with the University of Florida to research and develop next-generation gene therapy capsids with the goal of creating safer, more effective, and tissue-specific gene therapies. The expansion of this partnership will enable AavantiBio, a resident at The Hub, to further build out its platform focused on advancing innovative gene therapies in areas of significant unmet medical need.

The Adeno-associated virus (AAV) is the “delivery vehicle” for gene therapy, but the AAV’s capsid, or protein shell, is what steers the virus to the target cells and tissues, such as the heart, kidneys, lungs, and brain. As part of the strategic research collaboration focused on optimized genetic capsid codes, AavantiBio and the University of Florida will implement advanced cellular, molecular, and computational tools to develop next-generation AAV gene therapies. By utilizing machine learning and UF’s HiPerGator 3.0 supercomputer, the company is seeking to optimize genetic codes to create a pipeline of improved capsids for more effective and safer delivery for gene therapy.

“We are thrilled to build upon our partnership with the University of Florida and strengthen our commitment to developing the safest and most effective gene therapies to help patients with rare genetic diseases,” said Bo Cumbo, president and chief executive officer of AavantiBio. “The smallest changes in the genetic code of gene therapy capsids have the potential to dramatically improve biodistribution and efficacy to targeted tissues. We look forward to pursuing this exciting research as we aim to build a sustainable platform approach beginning with our lead program in Friedreich’s Ataxia, and currently extending into other complex disease areas where there is a high unmet need.”

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