Our integrated AAV discovery process is designed to produce optimized gene therapies
Our technologies aim to improve manufacturing fidelity and to minimize the risks of immunogenicity and toxicity
Our one-time gene therapy candidates are configured to fundamentally change how many diseases are treated
We identify novel AAV capsid variants at substructure- and cells-specific resolution to advance gene therapies with increased potency and specificty
Identify disease- and target-specific substructure
Select optimal route for clinical administration (RoA)
Our proprietary platforms enable discovery of novel tissue- and cell-specific capsids
Engineer specific payload expression using proprietary promoters and regulatory elements
Multiple campaigns have identified unique AAV capsid variants with ideal characteristics to address specific diseases
Deep Brain
Ependyma
Ear
Pan-Neuronal
Eye
muscle
Heart
kidney
Our novel AAV capsid variants have the potential to unlock significant clinical benefit and commercial upside
NHP screens for unique delivery zip codes coupled with computational models to optimize AAV gene therapies for virtually any tissue or cell type
NHP screens for unique delivery zip codes coupled with computational models to optimize AAV gene therapies for virtually any tissue or cell type
Redefining AAV: high precision,low dose, rapid manufacturing
By employing proprietary AAV capsid variants with enhanced potency and specificity, our gene therapy candidates are designed to reduce dose requirements and to improve safety, efficacy, manufacturing, and costs
We engineer capsids matched to optimized routes of administration to reduce AAV doses
Latus’ approach enables massive reductions in AAV manufacturing requirements
Uniquely competitive offering to advance AAV therapeutics from ultra-rare to common disease indications