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REGENERA MS

Financiado

Cerrado

Neuroregenerative peptide treatment for multiple sclerosis

REGENERA MS will assess the technical and commercial feasibility of a novel peptide as a superior treatment for multiple sclerosis (MS). Successful commercialization of our peptide could reduce the socioeconomic burden of MS, prov... ver más

31/12/2025

HELSINGIN YLIOPIST...

150K€

Presupuesto del proyecto: 150K€

Líder del proyecto

HELSINGIN YLIOPISTO No se ha especificado una descripción o un objeto social para esta compañía.

TRL 4-5

Fecha límite participación Sin fecha límite de participación.

Financiación concedida El organismo HORIZON EUROPE notifico la concesión del proyecto el día 2024-02-12

ERC-2023-POC: ERC PROOF OF CONCEPT GRANTS Objective:Objectives:The ERC Proof of Concept Grants aim at facilitating exploration of the commerci...

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Cerrada hace 2 años

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Información adicional privada

No hay información privada compartida para este proyecto. Habla con el coordinador.

1 Participantes

HELSINGIN YLIOPISTO

150.00K€ | Lider

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Duración del proyecto: 22 meses Fecha Inicio: 2024-02-12
Fecha Fin: 2025-12-31

Líder del proyecto

HELSINGIN YLIOPISTO No se ha especificado una descripción o un objeto social para esta compañía.

TRL 4-5

Presupuesto del proyecto 150K€

Fecha límite de participación Sin fecha límite de participación.

Descripción del proyecto REGENERA MS will assess the technical and commercial feasibility of a novel peptide as a superior treatment for multiple sclerosis (MS). Successful commercialization of our peptide could reduce the socioeconomic burden of MS, provide an early-therapy option to delay disease progression and thus extend and improve patients’ lives, with potential effectiveness in related neurodegenerative diseases. MS is a chronic inflammatory, autoimmune, and neurological disease without a cure, affecting the lives of 1.2M Europeans and causing significant economic costs to patients and society. Currently, there is no cure for MS. Approved disease-modifying treatments such as IFN-β1, glatiramer acetate and alemtuzumab are clinically effective but come with high costs, significant side-effects, and intrusive administration. Thus, a medical unmet need remains for novel MS therapies that can halt progression, promote myelin repair and limit complications. To improve on the current therapeutic regimen, we propose a next-generation neurotrophic factor (NTF) therapy that has curative potential by halting MS progression and regenerating demyelinated tissue. My group has discovered a novel peptide with neurotrophic properties and which, in contrast to classical NTFs, (i) has neurorestorative effects and can enhance remyelination (ii) penetrates the blood-brain barrier (BBB), (iii) can be subcutaneously administered, and (iv) can be inexpensively produced. In REGENERA MS, we will evaluate the pharmacokinetic properties and efficacy of a novel therapeutic peptide in organotypic brain cultures, human induced oligodendrocyte-like pluripotent stem cell-derived cells and in MS animal models. Subsequently, we will verify the IP position and strategy, perform an in-depth market and competitor analysis, and finally consolidate these findings into a business case to establish the best path to commercialization.

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