MARKET POTENTIAL

Driven by our global team of experts, Flavivaccine aims to create a safe and cost-effective vaccine against emerging global health threats

The project encompasses the entire value chain from basic science research institutions to private companies. The involvement of a vaccine developer and other key stakeholders will ensure the seamless transition of the vaccine candidate from pre-clinical investigation to clinical development. As illustrated below, the phases leading to commercialisation are:

6

Commercialisation

large sclae manufacturing and distribution of the approved vaccine worldwide.

6
Commercialisation

1

Target identification

studying the mechanisms of flavivirus diseases and identifying potential targets for a vaccine.

1
Target identification

2

Pre-clinical studies

evaluating safety, immunogenicity and efficacy of the vaccine candidates in animal models of flaviviral infection.

2
Pre-clinical studies

3

Vaccine candidate

identifying the candidate that has shown promise in pre-clinical studies.

3
Vaccine candidate

4

Clinical studies

assessing the vaccine's safety, immunogenicity and efficacy in human trials (phase I to Phase III)

4
Clinical studies

5

Market Approval

determining if the vaccine meets standards before it can be distributed to the public.

5
Market Approval

Through the design of comprehensive to-market strategies, strategic patenting, and collaboration with potential investors, Flavivaccine aims to start clinical evaluation right after the end of the project and to deliver a broad-spectrum flavivirus vaccine solution to populations worldwide at risk of mosquito-borne flavivirus infections.

The project will ultimately offer a global opportunity by protecting individuals worldwide against a broad range of flaviviruses including but not limited to dengue, yellow fever, Zika and West Nile viruses, and a multi-market potential, as both a travel vaccine, protective vaccine in endemic areas and pandemic response strategy.

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