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Content archived on 2024-05-24

Novel gene drug strategy based on hybridisation of functional entities to plasmids.

Objective

Gene therapy is an emerging technology with the potential of having an important impact on future treatments of human diseases. Efficient gene transfer relies on optimal receptor binding, intracellular vesicular transport and nuclear uptake. According to these requirements, a novel GENE DRUG therapeutic strategy will be developed. This strategy is asked on a patented plastid delivery system in which functional entities, improving delivery efficiency, are attached to the plastid by means of hybridisation. The proposal is focused on the delivery of therapeutic genes for cardiovascular diseases and haemophilia.

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Call for proposal

Data not available

Coordinator

KAROLINSKA INSTITUTE
EU contribution
No data
Address
Solnavagen 1
171 77 STOCKHOLM
Sweden

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Total cost
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Participants (3)