Scadenza: 15 December 2021
Scadenze successive:
by November 25th, 2021, applicants should:
- register on the TeTra portal at https://projects.telethon.it
- submit the project’s title
- fill in the Type of Research section, providing the name and code of the disease, the Research Type and Research Step
Topic:
The initiative aims at funding one-year seed research projects with a maximum budget of 50,000 €. These calls will give the opportunity to generate data and create new knowledge to pave the road for the development of new therapeutic approaches.
Agreements with Patient’s Associations have been reached for monothematic research calls on the following diseases:
- Spastic ataxia of Charlevoix-Saguenay (ARSACS) in partnership with Associazione Arsacs odv
- PIGA deficiency or Multiple Congenital Anomalies-Hypotonia-Seizures syndrome type 2 (MCAHS2) in partnership with A.Ge.P.I. odv
- Dejerine-Sottas disease (Charcot-Marie-Tooth disease type3) caused by the PMP22 Ser72Leu mutation
vascular Ehlers-Danlos syndrome (vEDS) in partnership with Con Giacomo contro Elhers Danlos Syndrome vascolare-APS
Ente finanziatore:
Fondazione Telethon
Who can participate:
Italian investigators - working either in public or private Italian non-profit research Institutions are eligible irrespectively of their funding status with Fondazione.
Status:
Closed
Quota finanziabile:
Maximum budget of 50,000 €
Topic:
The initiative aims at funding one-year seed research projects with a maximum budget of 50,000 €. These calls will give the opportunity to generate data and create new knowledge to pave the road for the development of new therapeutic approaches.
Agreements with Patient’s Associations have been reached for monothematic research calls on the following diseases:
- Spastic ataxia of Charlevoix-Saguenay (ARSACS) in partnership with Associazione Arsacs odv
- PIGA deficiency or Multiple Congenital Anomalies-Hypotonia-Seizures syndrome type 2 (MCAHS2) in partnership with A.Ge.P.I. odv
- Dejerine-Sottas disease (Charcot-Marie-Tooth disease type3) caused by the PMP22 Ser72Leu mutation
vascular Ehlers-Danlos syndrome (vEDS) in partnership with Con Giacomo contro Elhers Danlos Syndrome vascolare-APS
Who can participate:
Italian investigators - working either in public or private Italian non-profit research Institutions are eligible irrespectively of their funding status with Fondazione.
Programme:
Consortium:
Status: Open
Total budget:
Funding rate:
Maximum budget of 50,000 €
Notes:
Each researcher can apply, as Lead Applicant or as Collaborator, to one of the 4 Seed Grant Calls only.
