Community Research and Development Information Service - CORDIS

Horizon 2020 project information and now also report summaries are available on CORDIS. All H2020 projects can be downloaded from the EU Open Data Portal .

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The overall objective is to implement a European Joint Programme (EJP) Cofund for Rare Diseases which would create a research and innovation pipeline ""from bench to bedside"" ensuring rapid translation of research results into clinical applications and uptake in healthcare...
Record Number: 703070
The aim of this research should be to apply genomics and/or other –omics and/or other high-throughput approaches for the molecular characterisation of rare diseases in view of developing molecular diagnoses for a large number of undiagnosed rare diseases. Undiagnosed rare...
Record Number: 701969
ERA-NET rare disease research implementing IRDiRC objectives
ID: 643578
Start date: 2014-12-01, End date: 2019-11-30
Rare diseases (RD) are diseases that affect not more than 5 per 10 000 persons (according to the EU definition). 7000 distinct rare diseases exist, affecting between 6% and 8% of the population (about 30 million EU citizens). The lack of specific health policies for rare...
Programme: H2020-EU.3.1.
Record Number: 194080
Last updated on: 2017-08-22
Development of an innovative gene therapy platform to cure rare hereditary muscle disorders
ID: 667751
Start date: 2016-01-01, End date: 2019-12-31
The objective of MYOCURE is to develop an innovative gene therapy platform to cure rare hereditary muscle disorders, specifically focusing on myotubular myopathy (MTM) and glycogen storage disorder (GSD) type II. These are attractive diseases for gene therapy since they...
Programme: H2020-EU.3.1.3.
Record Number: 199738
Last updated on: 2016-11-29
Empowering Rare Disease Patients: Integrated Personalized Cloud Patient Monitoring Platform
ID: 662638
Start date: 2015-02-01, End date: 2015-04-30
We own and run a cloud patient monitoring platform that consists of one part for healthcare professionals: uClinics and another one for patients: uPatient. uClinics allows doctors to prescribe and assess the patient and uPatient empowers patients to understand their health...
Programme: H2020-EU.2.1.1.
Record Number: 196186
Last updated on: 2015-03-25
Heart On chip based on induced pluripotent Stem cell Technology for personalized Medicine
ID: 778354
Start date: 2018-01-01, End date: 2021-12-31
Many rare diseases cause chronic health problems or are even life-threatening. The impact on the quality of life of affected patients, of whom many are children, is significant. To date, a limited but increasing number of so-called orphan drugs (drugs for rare diseases) are...
Programme: H2020-EU.1.3.3.
Record Number: 212476
Last updated on: 2017-10-31
New therapies for rare diseases: New EU project MYOCURE advances treatment of rare hereditary muscle disorders
Vrije Universiteit Brussel (VUB) coordinates new Horizon2020 research initiative on the development of novel therapies for patients suffering from rare muscle diseases. MYOCURE is funded with €6 million by the European Commission and involves 8 European partner institutions. ...
Programme: H2020-EU.3.1.
Record Number: 130654
Last updated on: 2016-02-02
Support will be provided to clinical trials on substances where orphan designation has been given by the European Commission, where the proposed clinical trial design takes into account recommendations from protocol assistance given by the European Medicines Agency, and where...
Record Number: 701988
Smart multifunctional GLA-nanoformulation for Fabry disease
ID: 720942
Start date: 2017-01-01, End date: 2020-12-31
Lysosomal storage disorders (LSD) diseases are a group of rare diseases that currently lack a definitive cure. LSD incidence is about 1:5,000 - 1:10,000, representing a serious global health problem. In the case of Fabry LSD Disease (FD), the deficiency in α-Galactosidase A...
Programme: H2020-EU.2.1.2.
Record Number: 206748
Last updated on: 2017-04-12
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List retrieved on: 2018-12-11
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