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Country: United Kingdom
145 Projects, page 1 of 29
  • Funder: EC Project Code: 219707
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  • Funder: EC Project Code: 606577
  • Funder: EC Project Code: 733176
    Overall Budget: 4,113,380 EURFunder Contribution: 4,113,380 EUR

    Rabies is the deadliest disease on earth (99.9% fatality rate). Annually, ~58.000 people die from rabies, more than half of them are children. Many remain unvaccinated because of the high costs and the need for a cold-chain. Likewise, despite the existence of an excellent yellow fever (YF) vaccine, yearly ~30.000 people die of YF. The 80-year old low-tech production process does not allow to produce sufficient doses. There is now a real danger that major YF-outbreaks become uncontrollable. We aim at developing an efficient, safe, cheap, thermostable and easy-to-produce vaccine that can be needle-free administered, that protects against both rabies and YF, and that can be implemented in routine prophylactic paediatric vaccination. For this, we will employ our (P01a) proprietary infectious DNA (iDNA) vaccine technology. Simple, even needle-free injection of a low dose (1-10µg) of this easy-to-produce naked plasmid in mice and hamsters launches the YF vaccine virus and protects hamsters as efficiently as the commercial vaccine against lethal YF challenge. The iDNA YF vaccine will be used as vector to express relevant protective rabies antigens. Dual protection of such chimeric iDNA rabies/YF vaccine will be demonstrated against lethal rabies and YFV challenge in small animal models. Likewise, chimeric rabies/Japanese encephalitis and rabies/Zika virus iDNA vaccine candidates will be generated using this versatile platform. Next, induction of protective immunity will be demonstrated in rhesus macaques. The iDNA vaccines combine the benefits of both the YF live-attenuated vaccine (highly efficient life-long induction of immunity) and the thermo-stability, ease-of-production and the potential to customize (in response to emerging medical needs) of “classical” DNA vaccines. A path towards advanced pre-clinical and clinical development of such novel vaccines will be developed in compliance with European regulatory and WHO prequalification requirements.

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  • Funder: EC Project Code: 257669
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  • Funder: EC Project Code: 727494
    Overall Budget: 3,585,380 EURFunder Contribution: 2,999,440 EUR

    Animal diseases can cause serious social, economic and environmental damage, impact on animal welfare and in some cases directly threaten human health. The objective of SIRCAH (Secretariat for the International Research Consortium on Animal Health) is to provide organisational, communication and technical support to the STAR-IDAZ International Research Consortium (IRC) on Animal Health and thereby accelerate the development of much needed disease control tools. The agreed aim of STAR-IDAZ IRC is to coordinate research at international level to contribute to new and approved animal health strategies for at least 30 priority diseases/infections/issues. The deliverables will include candidate vaccines, diagnostics, therapeutic, procedures and key scientific information/tools to support risk analysis and disease control. To achieve these goals SIRCAH will support the IRC in establishing and running: i) Working Groups consisting of researchers for each of the priority topics and ii) a Scientific Committee, consisting of independent experts, who will advise the IRC Executive Committee. SIRCAH will provide the Working Groups with literature reviews and support them with gap analyses and the development of research roadmaps, map current activities against research needs and make recommendations relating to programme alignment, support the Scientific Committee and Executive Committee logistically, monitor progress against delivery targets and facilitate information exchange within and between all three levels

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