top of page

Delivering on the promise of gene therapy

With a groundbreaking, fully scalable cell-free viral vector technology

Challenge

In over hundreds of gene therapy clinical trials,  viral vectors such as Adeno-Associated Viruses (AAVs) are used to deliver healthy genes directly into cells, offering the potential to cure diseases, not just treat the symptoms.

But making these AAVs still rely on outdated, cell-based systems built for another era. The result: inconsistent quality, low potency, and slow, expensive development that holds back the field.

Cell based filling_edited.png

Solution

image.png

​At Fuse, we make AAVs outside the cell. 

Fuse cell-free technology replaces standard cell-based process with a precise enzymatic system that produces high-quality AAVs in a single step, delivering >99% filled capsids with unmatched purity and consistency.

Vision

We aim to redefine how gene therapies are made, to build a future where safe, potent, and scalable treatments reach patients faster. 

No cells. No bottlenecks. Just a faster path to better gene therapies.

image.png

Follow us:

  • LinkedIn

Contact us

©2024 BY FUSE VECTORS.

bottom of page