minority diseases

Investigating Fragile X syndrome in girls and adolescents
Investigating Fragile X syndrome in girls and adolescents 1080 608 Oriol Capell
As part of World Minority Disease Day, we are publishing the second installment of the 'Presenta la teva tesi' series. Lorena Joga, child and youth neuropsychologist at Parc Taulí and researcher at the I3PT explains what Fragile X Syndrome is and how it affects girls and teenagers. read more
I3PT, CONNECTA Therapeutics, CRG and IMIM receive 2,7 million from the Ministry of Science and Innovation to start Phase IIa of the drug CTH120 for fragile X syndrome
I3PT, CONNECTA Therapeutics, CRG and IMIM receive 2,7 million from the Ministry of Science and Innovation to start Phase IIa of the drug CTH120 for fragile X syndrome 1080 608 Mireia Córcoles
The Phase IIa study will evaluate the efficacy of CTH120 as an innovative therapy in adult patients with FXS, the most common form of inherited intellectual disability without a specific treatment read more
The I3PT wins 2 scholarships from the Ministry for a value of more than 700.000 euros
The I3PT wins 2 scholarships from the Ministry for a value of more than 700.000 euros 1080 608 Oriol Capell
The endowment will serve to finance the clinical trial of an innovative therapy for patients with Fragile X Syndrome and the discovery and clinical development of new PDE-10 inhibitors for the treatment of Prader-Willi syndrome read more
Parc Taulí organizes the first European Workshop on Angelman Syndrome in Catalonia
Parc Taulí organizes the first European Workshop on Angelman Syndrome in Catalonia 1080 608 Mireia Córcoles
The aim of the first edition of the EWAS was to improve the clinical approach and research of this minority disease read more
A cystic fibrosis project of the I3PT, winner of the Pau Massana Grant
A cystic fibrosis project of the I3PT, winner of the Pau Massana Grant 1080 608 Mireia Córcoles
The Cellers Maset scholarship is endowed with €25.000, and will allow funding each year for a research project on minority diseases read more
Cellers Maset creates the Pau Massana Scholarship for the research of minority diseases of the I3PT
Cellers Maset creates the Pau Massana Scholarship for the research of minority diseases of the I3PT 1080 608 Mireia Córcoles

The entity has signed a collaboration agreement with the Parc Taulí Research and Innovation Institute to raise funds through a solidarity wine initiative, and to contribute €25.000 annually for research into minority diseases Cellers Maset and the Parc Taulí Research and Innovation Institute (I3PT) have signed a collaboration agreement for the creation of the first Pau Massana Scholarship for Rare Diseases. This scholarship is an initiative of the winery for…

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