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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.

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

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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