Explore the words cloud of the FIDA project. It provides you a very rough idea of what is the project "FIDA" about.
The following table provides information about the project.
| Coordinator |
FIDA-TECH APS
Organization address contact info |
| Coordinator Country | Denmark [DK] |
| Total cost | 3˙451˙604 € |
| EC max contribution | 2˙603˙936 € (75%) |
| Programme |
1. H2020-EU.3. (PRIORITY 'Societal challenges) 2. H2020-EU.2.1. (INDUSTRIAL LEADERSHIP - Leadership in enabling and industrial technologies) |
| Code Call | H2020-EIC-FTI-2018-2020 |
| Funding Scheme | IA |
| Starting year | 2019 |
| Duration (year-month-day) | from 2019-12-01 to 2021-11-30 |
Take a look of project's partnership.
| # | ||||
|---|---|---|---|---|
| 1 | FIDA-TECH APS | DK (ROSKILDE) | coordinator | 1˙394˙621.00 |
| 2 | FACHHOCHSCHULE NORDWESTSCHWEIZ | CH (WINDISCH) | participant | 626˙043.00 |
| 3 | ELVESYS | FR (PARIS) | participant | 340˙105.00 |
| 4 | NOVOPTIM SARL | FR (PARIS) | participant | 243˙166.00 |
Therapeutic antibodies have rapidly become a major component of modern medicine. The global research antibodies market size is expected to reach €3.8bn by 2025. However, exiting research tools have not been able to eliminate Hyper-Sensitivity Reactions (HSRs) against the biologic drug by the patient’s immune system. HSRs are estimated to occur in 10-15% of hospital patients and can arise for any biologic, mostly antibodies. Antibodies are also important in the R&D of new vaccines. To test vaccines, it is necessary to follow the generation of auto-antibodies to verify that the vaccine is working well. This analysis is done with the same tools used in the antibodies research, and with the same drawbacks: artificial assays based on non-native sample materials. Vaccine R&D is immensely costly: up to €400m over a 11-year timeline is standard for a completely new vaccine and overall failure rate from preclinical through to registration is 94%. FIDA is a patented solution that simplifies and standardises immunological measurements under native conditions. We go from 15 treatment steps on current platforms to a single step with FIDA. FIDA is a powerful methodology for quantifying and characterising antibodies and antibody binding with up to 10-times higher sensitivity than present tools. Assays take 5-20 minutes to run, 90% less than alternatives, with full walk-away automation as-standard. FIDA’s simplicity allows to set-up assays versus new targets within 1 day versus 10 days with current tools. It is based on a microcapillary system that needs <3μl of sample, 16-times less than today’s methods to support parallel testing of multiple early-pipeline drug samples. FIDA uses up to 10μl of standard reagents and running costs are €2.60/assay, saving 61% in operational costs. FIDA focuses on both the global research antibodies market and vaccine R&D market at pre-clinical phase (in which certification as a diagnostic/prognostic device is not needed).
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The information about "FIDA" are provided by the European Opendata Portal: CORDIS opendata.
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