Private
C.H.I.CO. Cluster of Health Innovation and Community, Cluster of regione Lazio in Italy, Private organization to help Life Science Actors
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LifeArc (MRC-Translation gap funding)
Published by OXFORD INVENTION FUND (OIF)
Basic ResearchClinical ReasearchIndustrial Development or SMEPreclinical ResearchPrivate
Sanofi Innovation Awards iAwards Europe
Published by SANOFI
AwardBasic ResearchClinical ResearchPreclinical ResearchPrivateLaunched in the US three years ago, Sanofi’s Innovation Awards (iAwards) program is now expanding into Europe. Developed in response to the continuing rise of chronic diseases worldwide, the iAwards aim to promote scientific breakthroughs by tapping into the world’s greatest minds through close collaboration with renowned academic institutions.
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Towards a Concrete Improvement in the Quality of Life of Patients with Autoimmune Myasthenia
Published by FONDATION MALADIES RARES
Autoimmune MyastheniaThe Fondation Maladies Rares and UCB have joined forces to offer a €30, 000 research grant to a humanities and social sciences (HSS) research project focused on findingconcrete, short-term ways ofimproving the life course of patients suffering from generalized autoimmune myasthenia gravis.
The grant will be awarded to a research project focusing on the individual, family and/or social consequences specifically linked to generalized autoimmune myasthenia gravis, in order to gain a better understanding of the impact of this disease, and in particular muscular fatigability, on quality of life at the level of the individual, couple or family, for example.
View this resource Bookmark this resourceThe Fondation Maladies Rares is pleased to announce the launch of its “GenOmics” 2024 call for projects.
The aim of this AAP is to support hypothesis-driven research projects aimed at exploring the genetic and molecular basis of rare diseases using NGS approaches (WES, WGS, RNA-seq, small RNA-seq, ChIP-seq, Methyl-seq, etc.).
Support from the Fondation Maladies Rares will give project leaders access to innovative high-throughput sequencing technologies for the analysis of exomes, genomes, transcriptomes or epigenomes.
View this resource Bookmark this resourceFunding is key when it comes to developing an idea or research result. Every year, KTH Innovation helps KTH projects secure over 40 million SEK in funding.
View this resource Bookmark this resourceThe Chan Zuckerberg Initiative invites applications for five-year projects from patient-led rare disease advocacy organizations to join the Rare As One Network. Grantee organizations will accelerate research within individual disease areas and work across specified areas of scientific focus (channelopathies; ciliopathies; or inborn errors of metabolism) to develop shared research priorities and proposals.
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Sanofi iAwards Europe
Published by SANOFI
Cell and Gene TherapiesImmunologyInflammatory DiseasesOncologyRare and Neurological DiseasesA booster to transform groundbreaking ideas in the field of target identification, disease knowledge and translational science into innovative therapeutic solutions. We partner with best-in-class academics to serve a common goal: accelerating innovation for patients.
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