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Introducing the next-generation AAV-targeting platform

Tavira Therapeutics' innovative platform represents a unique breakthrough in AAV gene delivery


We are developing an innovative process that equips recombinant AAV vectors with molecules that accurately target them towards their intended locations.

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How it works

How it works

We engineer a well-characterized parental AAV serotype to contain an enzyme recognition site.  

​decorated AAV, dAAVe

Via enzymatic conjugation, we attach specific targeting groups.

Those could be chemical (small molecule) or biological
(e.g., nanobody, peptide, antibody fragment).

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Advantages

Advantages

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Increased specificity

Our technology precisely targets specific human tissues or cell types, enhancing therapeutic outcomes while minimizing unwanted effects.

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Higher potency

With improved efficacy, our decorated AAV particles require a lower dose to achieve clinical benefits, reducing the overall treatment burden.

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Better manufacturing

Our platform ensures robust and scalable manufacturing processes, enabling consistent production at a higher standard.

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Improved toxicity profile

Our technology significantly reduces off-target effects, improving safety for patients.

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Lower cost

Efficient production and lower dosing result in shorter development timelines and reduced costs, making treatments accessible to a wider range of patients and conditions beyond rare diseases.

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