At AVROBIO, we aim to halt or reverse disease with a single dose of gene therapy. ONE COMPANY with a vision to bring personalized gene therapy to the world. Our goal is simple and powerful: We aim to enable individuals with genetic disease to live longer free from disease progression, free from painful and debilitating symptoms and free from the burden of chronic treatment regimens.
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- Business Type:
- Industry Type:
- Medical Research
- Market Focus:
- Globally (various continents)
The life-limiting symptoms patients with these disorders experience are caused by the lack of a crucial functional protein. Our personalized approach to gene therapy starts with inserting a therapeutic gene in the patient’s own stem cells to enable production of the protein they lack. Over time, these cells are expected to multiply and produce daughter cells. Each new generation of daughter cells is expected to contain the therapeutic gene.
This approach holds the potential for the all-important protein to be durably expressed throughout the patient’s body, including the brain, delivering freedom for life.
Our initial focus is on lysosomal disorders, where the standard of care does not halt disease progression or adequately address many symptoms, particularly in the brain and nervous system. Our investigational therapies are currently being studied in clinical trials in Fabry disease, Gaucher disease and cystinosis. We are also advancing a program in Pompe disease.