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Unité de recherche
INNOSUISSE
Numéro de projet
14340.1;7 PFLS-LS
Titre du projet
IFNy-neutralizing peptides to treat Amyotrophic Lateral Sclerosis (Feasibility study)
Titre du projet anglais
IFNã-neutralizing peptides to treat Amyotrophic Lateral Sclerosis (Feasibility study)

Textes relatifs à ce projet

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Description succincte
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Résumé des résultats (Abstract)
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Textes saisis


CatégorieTexte
Description succincte
(Anglais)
IFNã-neutralizing peptides to treat Amyotrophic Lateral Sclerosis (Feasibility study)
Description succincte
(Français)
IFNy-neutralizing peptides to treat Amyotrophic Lateral Sclerosis (Feasibility study)
Résumé des résultats (Abstract)
(Anglais)
The proposed feasibility study concerns the development of a novel synthetic drug for Amyotrophic Lateral Sclerosis and Parkinson disease. Lascco¿s program on neurodegenerative diseases targets IFNã-mediated death pathways and neuroinflammation. This study aims at providing critical data on the identification and selection of small peptides with high affinity, stability, and biocompatibility, and with the unique ability to induce IFNã neutralization. The two best hit compounds will then, in a subsequent phase, be integrated in polymer delivery platforms and evaluated in vivo
Résumé des résultats (Abstract)
(Français)
The proposed feasibility study concerns the development of a novel synthetic drug for Amyotrophic Lateral Sclerosis and Parkinson disease. Lascco¿s program on neurodegenerative diseases targets IFNã-mediated death pathways and neuroinflammation. This study aims at providing critical data on the identification and selection of small peptides with high affinity, stability, and biocompatibility, and with the unique ability to induce IFNã neutralization. The two best hit compounds will then, in a subsequent phase, be integrated in polymer delivery platforms and evaluated in vivo