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CRUZIVAX SIGNED

Vaccine for prevention and treatment of Trypanosoma cruzi infection

Total Cost €

0

EC-Contrib. €

0

Partnership

0

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 CRUZIVAX project word cloud

Explore the words cloud of the CRUZIVAX project. It provides you a very rough idea of what is the project "CRUZIVAX" about.

immunity    formulations    treatment    economics    humoral    11    needle    cruzivax    combined    million    drug    caused    mild    sequences    gap    burden    mass    chronic    engineered    trial    health    manufacturing    symptoms    safety    000    worldwide    locally    19    chagas    latin    21    efficacy    healthy    cruzi    formulation    antigen    suburban    morbidity    cardiac    lacking    cellular    therapeutic    acute    profile    carry    trypanosoma    30    countries    american    disease    stimulating    carriers    protect    social    parasitic    pipeline    became    settings    immune    restricted    performing    chimeric    benznidazole    first    structure    limited    therapy    infections    prophylactic    difficult    volunteers    trivalent    migration    efficient    clinical    usa    immunogenicity    strengthen    largely    dogs    preclinical    primates    activation    infection    chronicity    rural    vi    reducing    bridge    endemic    economic    human    proven    active    models    free    perform    poor    critical    facilitated    vaccine    adjuvant    gt    cgmp    conduct    interruption    unnoticed    americas    mice    self    reports    decoy   

Project "CRUZIVAX" data sheet

The following table provides information about the project.

Coordinator
HELMHOLTZ-ZENTRUM FUR INFEKTIONSFORSCHUNG GMBH 

Organization address
address: INHOFFENSTRASSE 7
city: BRAUNSCHWEIG
postcode: 38124
website: www.helmholtz-hzi.de

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 Germany [DE]
 Total cost 0 €
 EC max contribution 8˙391˙240 € (0%)
 Programme 1. H2020-EU.3.1.3. (Treating and managing disease)
 Code Call H2020-SC1-2018-Two-Stage-RTD
 Funding Scheme RIA-LS
 Starting year 2019
 Duration (year-month-day) from 2019-06-01   to  2024-05-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    HELMHOLTZ-ZENTRUM FUR INFEKTIONSFORSCHUNG GMBH DE (BRAUNSCHWEIG) coordinator 2˙070˙198.00
2    COMMISSARIAT A L ENERGIE ATOMIQUE ET AUX ENERGIES ALTERNATIVES FR (PARIS 15) participant 963˙795.00
3    ASA SPEZIALENZYME GMBH DE (WOLFENBUTTEL) participant 951˙500.00
4    ATRC AURIGON TOXICOLOGIAI KUTATOKOZPONT KORLATOLT FELELOSSEGU TARSASAG HU (DUNAKESZI) participant 863˙592.00
5    GENIBET - BIOPHARMACEUTICALS SA PT (OEIRAS) participant 861˙249.00
6    UNIVERSIDAD DE BUENOS AIRES AR (BUENOS AIRES) participant 745˙500.00
7    UNIVERSITEIT ANTWERPEN BE (ANTWERPEN) participant 577˙302.00
8    UNIVERSIDADE NOVA DE LISBOA PT (LISBOA) participant 442˙206.00
9    INSTITUTO DE BIOLOGIA EXPERIMENTAL E TECNOLOGICA PT (OEIRAS) participant 352˙356.00
10    VAKZINE PROJEKT MANAGEMENT GMBH DE (HANNOVER) participant 310˙137.00
11    FUNDACION PRIVADA INSTITUTO DE SALUD GLOBAL BARCELONA ES (BARCELONA) participant 253˙401.00

Map

 Project objective

Chagas is a neglected disease endemic in 21 Latin-American countries caused by Trypanosoma cruzi. It is the largest parasitic disease burden in the Americas (>11,000,000 chronic infections) and the first cause of cardiac morbidity in poor rural/suburban areas. It became a worldwide concern as a result of mass migration with reports in 19 non-endemic areas (>1.3 million carriers in EU/USA). Treatment is difficult since acute infections have mild symptoms and remain largely unnoticed evolving to chronicity. Drug therapy is also long, often associated with side effects (10-30% interruption) and only active during early infection. The main objective of CRUZIVAX is to bridge the gap between preclinical and clinical development by performing preclinical and clinical phase 1 studies of a needle-free vaccine against T. cruzi with proven efficacy in preclinical models. The vaccine is based on a structure-engineered trivalent chimeric antigen lacking immune decoy sequences and an adjuvant promoting self-limited locally-restricted immune activation stimulating humoral and cellular immunity, which is expected to protect as prophylactic or therapeutic (combined with Benznidazole) vaccine. To achieve this CRUZIVAX will: (i) conduct preclinical studies in mice to assess immunogenicity and efficacy of different vaccine formulations in prophylactic and therapeutic settings, (ii) analyse the immunogenicity and efficacy of the best vaccine formulation in dogs and non-human primates, (iii) produce cGMP antigen and adjuvant by cost-efficient manufacturing (facilitated uptake by health systems with limited resources), (iv) perform a preclinical safety assessment of the vaccine, (v) conduct a phase 1 vaccine clinical trial in healthy volunteers, and (vi) carry out a health economics analysis to identify critical target-product profile parameters. The vaccine will strengthen the pipeline of products for Chagas disease, aimed at reducing disease burden and its social and economic impact.

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

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