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

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Identify disease- and target-specific substructure
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Select optimal route for clinical administration (RoA)
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Our proprietary platforms enable discovery of novel tissue- and cell-specific capsids
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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

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Deep Brain
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Ependyma
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Ear
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Pan-Neuronal
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Eye
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muscle
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Heart
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kidney

Our novel AAV capsid variants have the potential to unlock significant clinical benefit and commercial upside

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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

*AAV Vector Market, Root Analysis, 2022
*AAV Vector Market, Root Analysis, 2022