Explore the words cloud of the TAT-CF project. It provides you a very rough idea of what is the project "TAT-CF" about.
The following table provides information about the project.
Coordinator |
UNIVERSIDAD DE BURGOS
Organization address contact info |
Coordinator Country | Spain [ES] |
Project website | http://www.tat-cf.eu |
Total cost | 4˙591˙287 € |
EC max contribution | 4˙591˙287 € (100%) |
Programme |
1. H2020-EU.3.1.3. (Treating and managing disease) |
Code Call | H2020-PHC-2015-two-stage |
Funding Scheme | RIA |
Starting year | 2016 |
Duration (year-month-day) | from 2016-01-01 to 2018-12-31 |
Take a look of project's partnership.
# | ||||
---|---|---|---|---|
1 | UNIVERSIDAD DE BURGOS | ES (BURGOS) | coordinator | 665˙563.00 |
2 | AVIDIN KUTATO, FEJLESZTO ES KERESKEDELMI KFT | HU (SZEGED) | participant | 732˙875.00 |
3 | CONSIGLIO NAZIONALE DELLE RICERCHE | IT (ROMA) | participant | 610˙273.00 |
4 | BIOKERALTY RESEARCH INSTITUTE AIE | ES (ARCAUTE ALAVA) | participant | 591˙875.00 |
5 | BIONEER A/S | DK (HOERSHOLM) | participant | 557˙375.00 |
6 | STEINBEIS INNOVATION GGMBH | DE (STUTTGART) | participant | 523˙953.00 |
7 | AGENCIA ESTATAL CONSEJO SUPERIOR DEINVESTIGACIONES CIENTIFICAS | ES (MADRID) | participant | 519˙368.00 |
8 | ISTITUTO GIANNINA GASLINI | IT (GENOVA) | participant | 390˙002.00 |
This project will develop an innovative therapeutic approach for the treatment of Cystic Fibrosis (CF). This condition originates from the defective function of the CFTR protein, a chloride and bicarbonate permeable transmembrane channel. This project will evaluate small molecules capable of facilitating the transmembrane transport of anions such as chloride and bicarbonate and will thus enable CF treatment by replacing the missing CFTR anion permeation activity. This represents an unexplored path in the treatment of CF and a paradigm shift with respect to current strategies searching for a cure for CF. Instead of focusing on the development of mutation-specific treatments, we plan to develop a therapy applicable to CF patients, regardless of the type of mutation they harbor. Thus, this therapeutic approach overcomes the limitation of current mutation-specific treatments and is applicable to CF patients in general. To achieve this goal we have set up a comprehensive program to validate a research concept and complete the preclinical development of a new lead compound, making it ready for early clinical development. A rmultidisciplinary team of qualified researchers have been assembled to bring to conclusion a truly translational project from the synthesis of new compounds to validation on animal models. Cystic Fibrosis affects more people than any other rare disease. Therefore, it could be said, at least in quantitative terms, that CF qualifies as the main target of the topic. This project aims to complete the preclinical development of novel, innovative drugs based on a radically new concept in Cystic Fibrosis therapies. This result fully addresses the expected impact set out in the work programme of advancing the development of new therapeutic options for patients living with rare diseases as well as contributing to reach the IRDiRC objective to deliver 200 new therapies for rare diseases by 2020.
Lung epithelial cells from F508del patients | Documents, reports | 2019-07-26 14:38:12 |
Biophysical and pharmacological characterisation of the anionophores | Documents, reports | 2019-07-26 14:38:13 |
Project Website | Websites, patent fillings, videos etc. | 2019-07-26 14:38:13 |
Anionophores in F508del and G551D mouse models | Documents, reports | 2019-07-26 14:38:13 |
Physiology of normal and cystic fibrosis bronchial epithelium; Imaging assay | Documents, reports | 2019-07-26 14:38:12 |
iPS cells from G551D patients | Documents, reports | 2019-07-26 14:38:12 |
iPS cells from F508del patients | Documents, reports | 2019-07-26 14:38:12 |
Intestinal organoids from G551D patients | Documents, reports | 2019-07-26 14:38:12 |
Calu-3 mutant CFTR F508del and G551D cells | Documents, reports | 2019-07-26 14:38:13 |
Intestinal organoids from F508del patients | Documents, reports | 2019-07-26 14:38:12 |
pH-insensitive Cl- sensor assay | Documents, reports | 2019-07-26 14:38:13 |
Lung epithelial cells from G551D patients | Documents, reports | 2019-07-26 14:38:13 |
Correlation of anion transport activity with mucin release in Calu-3 CFTR wt and mutant sensor cell lines | Documents, reports | 2019-07-26 14:38:12 |
Take a look to the deliverables list in detail: detailed list of TAT-CF deliverables.
year | authors and title | journal | last update |
---|---|---|---|
2018 |
Aarne Fleischer, Iván M. Lorenzo, Esther Palomino, Trond Aasen, Fernando Gómez, Miguel Servera, VÃctor J. Asensio, VÃctor Gálvez, Juan Carlos Izpisúa-Belmonte, Daniel Bachiller Generation of two induced pluripotent stem cell (iPSC) lines from p.F508del Cystic Fibrosis patients published pages: 1-5, ISSN: 1873-5061, DOI: 10.1016/j.scr.2018.03.004 |
Stem Cell Research 29 | 2019-07-26 |
2018 |
Ãngel del Pozo, Roberto Quesada, Manfred Frey 4th TAT-CF Newsletter published pages: , ISSN: , DOI: |
2019-07-26 | |
2018 |
Ãngel del Pozo, Roberto Quesada, Oscar Moran, Emanuela Caci, Manfred Frey, Daniel Bachiller, Anette Mullertz, Laszlo Puskas 6th TAT-CF Newsletter published pages: , ISSN: , DOI: |
2019-07-26 | |
2018 |
Ãngel del Pozo, Roberto Quesada 5th TAT-CF Newsletter published pages: , ISSN: , DOI: |
2019-07-26 | |
2018 |
Ãngel del Pozo, Roberto Quesada, Oscar Moran, Emanuela Caci 3rd TAT-CF Newsletter published pages: , ISSN: , DOI: |
2019-07-26 | |
2018 |
Elsa Hernando, Valeria Capurro, Claudia Cossu, Michele Fiore, MarÃa GarcÃa-Valverde, Vanessa Soto-Cerrato, Ricardo Pérez-Tomás, Oscar Moran, Olga Zegarra-Moran, Roberto Quesada Small molecule anionophores promote transmembrane anion permeation matching CFTR activity published pages: , ISSN: 2045-2322, DOI: 10.1038/s41598-018-20708-3 |
Scientific Reports 8/1 | 2019-07-26 |
2018 |
Claudia Cossu, Michele Fiore, Debora Baroni, Valeria Capurro, Emanuela Caci, Maria Garcia-Valverde, Roberto Quesada, Oscar Moran Anion-Transport Mechanism of a Triazole-Bearing Derivative of Prodigiosine: A Candidate for Cystic Fibrosis Therapy published pages: , ISSN: 1663-9812, DOI: 10.3389/fphar.2018.00852 |
Frontiers in Pharmacology 9 | 2019-07-26 |
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The information about "TAT-CF" are provided by the European Opendata Portal: CORDIS opendata.