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MultiViVax SIGNED

Development of Effective Vaccines against Multiple Lifecycle Stages of Plasmodium vivax malaria

Total Cost €

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EC-Contrib. €

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Partnership

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Project "MultiViVax" data sheet

The following table provides information about the project.

Coordinator
THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD 

Organization address
address: WELLINGTON SQUARE UNIVERSITY OFFICES
city: OXFORD
postcode: OX1 2JD
website: www.ox.ac.uk

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country United Kingdom [UK]
 Project website http://www.multivivax.eu
 Total cost 5˙763˙405 €
 EC max contribution 5˙058˙974 € (88%)
 Programme 1. H2020-EU.3.1.2. (Preventing disease)
 Code Call H2020-SC1-2016-RTD
 Funding Scheme RIA
 Starting year 2017
 Duration (year-month-day) from 2017-01-01   to  2021-12-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD UK (OXFORD) coordinator 4˙526˙425.00
2    GENOME RESEARCH LIMITED UK (LONDON) participant 351˙298.00
3    NOVAVAX AB SE (UPPSALA) participant 56˙250.00
4    OSIVAX SAS FR (PARIS) participant 35˙873.00
5    INSTITUT DE RECHERCHE POUR LE DEVELOPPEMENT FR (MARSEILLE) participant 30˙000.00
6    THE UNIVERSITY OF EDINBURGH UK (EDINBURGH) participant 30˙000.00
7    EXPRES2ION BIOTECHNOLOGIES APS DK (HORSHOLM) participant 25˙000.00
8    IMAXIO SA FR (PARIS) participant 4˙126.00

Map

 Project objective

Plasmodium vivax is the most widespread malaria and constitutes a significant proportion of human malaria cases. P. vivax accounts for 100-400 million clinical cases each year among the 2.5 billion people living at risk in Latin America, Oceania and Asia. The recently revised Malaria Vaccine Technology Roadmap to 2030 recognises the severity of P. vivax malaria and calls for a vaccine intervention to achieve 75% efficacy over two years – equally weighted with P. falciparum. However, despite this global health need, efforts to develop interventions against this parasite have lagged far behind those for P. falciparum, in large part because of critical bottlenecks in the vaccine development process. These include i) lack of assays to prioritise and down-select new vaccines due to lack of an in vitro P. vivax long-term culture system, and ii) lack of easy access to a safe controlled human malaria infection (CHMI) model to provide an early indication of vaccine efficacy in humans. The Objectives of this MultiViVax proposal will address these critical bottlenecks and shift the “risk curve” in order to better select successful vaccine candidates against multiple lifecycle stages of P. vivax:

1. We will establish a P. vivax CHMI model in Europe for the first time to facilitate the better selection of effective vaccines and remove the current bottleneck for their early-phase clinical testing.

2. We will utilise this CHMI model to identify novel antigens associated with protective blood-stage immunity in humans by taking advantage of recent advances in immuno-screening and parasite RNASeq.

3. We will progress existing vaccines targeting the current leading antigens for both the blood- and transmission-stages along the clinical development pipeline.

4. We will develop novel transgenic parasites for use in assays in order to overcome the current bottleneck in vaccine down-selection caused by the inability to culture P. vivax parasites.

 Deliverables

List of deliverables.
Generation and fitness assessment of transgenic parasite Pf-Pvs25 Documents, reports 2020-01-27 12:28:09
Description of website Websites, patent fillings, videos etc. 2020-01-27 12:28:09

Take a look to the deliverables list in detail:  detailed list of MultiViVax deliverables.

 Publications

year authors and title journal last update
List of publications.
2019 Thomas. A. Rawlinson, Natalie M. Barber, Franziska Mohring, Jee Sun Cho, Varakorn Kosaisavee, Samuel F. Gérard, Daniel G. W. Alanine, Geneviève M. Labbé, Sean C. Elias, Sarah E. Silk, Doris Quinkert, Jing Jin, Jennifer M. Marshall, Ruth O. Payne, Angela M. Minassian, Bruce Russell, Laurent Rénia, François H. Nosten, Robert W. Moon, Matthew K. Higgins, Simon J. Draper
Structural basis for inhibition of Plasmodium vivax invasion by a broadly neutralizing vaccine-induced human antibody
published pages: 1497-1507, ISSN: 2058-5276, DOI: 10.1038/s41564-019-0462-1
Nature Microbiology 4/9 2020-03-05

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The information about "MULTIVIVAX" are provided by the European Opendata Portal: CORDIS opendata.

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