We’re seeking to advance the standard for precision gene therapy

By deploying advanced computational methods and unbiased screening directly in NHP's - we're mapping the future of delivery for genetic medicines. Designed to accurately target tissues and reduce unwanted interactions, our technology aims to minimize the risks of immunogenicity and toxicity, delivering the payload exactly where it's needed.

Our novel capsid variants aim to enable one-time gene therapies to treat an unprecedented number of diseases

By developing more potent AAVs, our candidates are being designed to provide improved efficacy at low doses, potentially improving costs, manufacturing efficiency and patient safety.

Problems with AAV (high COGS, toxicity, variable efficacy) stem from high dose requirements

Latus reduces aav doses via direct routes of administration (RoA) and engineering capsids with disease-specific tropism

Latus’ approach enables massive reductions in AAV manufacturing requirements

Uniquely competitive offering to advance AAV therapeutics from ultra-rare to common disease indications