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INTEGRATED PROJECT

INTEGRATED PROJECT. MUVAPRED. Phase I trials in EU. Vaccine candidates. Antigens. Adjuvants. Delivery systems. Phase I trials in Africa. Pre-clinical testing. Mice. Vaccine candidates for EDCTP. Guinea Pigs (TB). Monkeys . New vaccines for poverty. MUVAPRED. Sub-project 1.

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INTEGRATED PROJECT

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  1. INTEGRATED PROJECT MUVAPRED Phase I trials in EU Vaccine candidates Antigens Adjuvants Delivery systems Phase I trials in Africa Pre-clinical testing Mice Vaccine candidates for EDCTP Guinea Pigs (TB) Monkeys New vaccines for poverty MUVAPRED Sub-project 1 Sub-project 2 Sub-project 3 Vaccine Candidates Animal studies Human studies Mice Guinea Monkeys Adjuvants Delivery Correlates GMP Phase I Antigens systems protection WP2 WP1 WP8 WP9 WP4 WP5 WP6 WP3 WP7 Indicative timelines of the main activities Development of new promising vaccine candidates (Subproject 1) Development of new promising vaccine candidates   Comparative testing in animal models Phase I trials in EU with available candidates Clinical trials in Africa Phase I clinical trials with new vaccine candidates Correlates of protection YEARS 1 2 3 4 5 MUCOSAL VACCINES FOR POVERTY-RELATED DISEASES MUVAPRED Project coordinator: R. Rappuoli, Chiron Srl EC contribution : 15.250.000 Euro Starting date: 1st December 2003 Duration: 5 years Participants: 24 from 10 countries Project Summary Human Immunodeficiency Virus and Mycobacterium tuberculosis enter the human body at mucosal sites. The aim of the present project is to develop mucosally delivered vaccines against HIV and TB which will induce local immunity able to neutralise the pathogens at their port of entry and systemic immunity able to prevent systemic spread of the infection. The possible development of mucosal vaccines against malaria will be also investigated. The trust of the project derives from the recent proof of concept that mucosal vaccines are feasible in humans. While the first trials are performed, new systems to deliver mucosal vaccines and basic mechanisms of mucosal immune responses and memory in humans will be studied. This will allow better understanding of the clinical results and optimisation of second generation vaccines to be tested in Developing Countries during the second phase of the project. Project structure • Objectives • Phase I clinical trials in Europe with the available mucosal antigens against HIV/AIDS and TB (two to three vaccine candidates). • Second generation, optimised vaccine candidates against HIV/AIDS, TB and malaria (antigens, adjuvants, delivery systems). • Selection of the most promising vaccine candidates by comparative testing in animal models • Phase I clinical trials in Europe with new vaccine candidates developed by the consortium • Phase I clinical trials in Africa with the vaccine candidates that have proven to be safe and immunogenic in the first clinical trials in Europe Scientific and Administrative Management Participants Chiron Italy, Imperial College of Science UK, University of Goteborg Sweden, University of Siena Italy, Institute Pasteur France, Istituto Superiore di Sanità Italy, Institute for Research in Biomedicine CH, Max-Planck-Institute, Germany University Hamburg Germany,Trinity College Dublin Ireland, Serum State Institute Denmark, Consiglio Nazionale delle Ricerche Italy, Istituto Humanitas Milano Italy, German Arthritis Research Center DRFZ Germany, St George’s Vaccine Institute UK, Institute of Microbiology Czech Republic, CAMR UK, University of Florence Italy, Centre-Hospitalier-Universitaire Ignace Deen Guinea, University of Lausanne Switzerland, ALTA Srl Italy, LIONEX Diagnostic & Therapeutics GmbH Germany, INOTECH AG Switzerland STEERING COMMITTEE R. Rappuoli R. Rappuoli, Chiron EXTERNAL D. Medaglini Project Coordinator ADVISORY EU Sci. Officer P. Andersen BOARD D. Medaglini A. Tagliabue, ALTA G. Dougan Administrative Manager University of Siena J. Holmgren S.H.E. Kaufmann Scientific Manager COORDINATING TEAM A. Lanzavecchia D. Lewis T. Lehner G. Pozzi web site: http://www.mucosalimmunity.org/muvapred/

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