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Gene Therapy for treatment of rare inherited Arrhythmogenic Cardiomyopathy

Descrizione del progetto

Il cuore del problema: terapia genica mirata per la cardiomiopatia aritmogena

Lo sviluppo di trattamenti per le malattie cardiache rare è spesso lento e costoso a causa dell’insufficiente conoscenza del funzionamento di queste patologie. Il progetto GEREMY, finanziato dall’UE, mira a superare questo problema creando una terapia genica curativa per la cardiomiopatia aritmogena (arrhythmogenic cardiomyopathy, ACM) ereditaria. Targhettizzando specifiche mutazioni genetiche (PLN e PKP2), i ricercatori utilizzano metodi avanzati di editing genico e di somministrazione per correggere i difetti e ripristinare la funzione del muscolo cardiaco. Il progetto svilupperà anche nuovi modelli di malattia, garantirà la sicurezza attraverso test rigorosi, si preparerà a future sperimentazioni cliniche e si allineerà alle esigenze dei pazienti. In definitiva, GEREMY mira a trasformare l’assistenza ai pazienti, riducendo in modo significativo gli oneri sanitari e fornendo una tabella di marcia per il trattamento di altre patologie cardiache genetiche.

Obiettivo

Development of a cure for rare cardiac diseases is a risky, costly and time-consuming process, which is hampered by insufficient insight into pathophysiological mechanisms of the diseases and lack of relevant disease models.
The GEREMY consortium proposes to overcome this challenge by developing a gene therapy (GT) for inherited arrhythmogenic cardiomyopathy (ACM), by targeting the disease-causing PLN (non-desmosomes) and PKP2 (cardiac desmosomes) mutations. The GEREMY consortium will apply a unique parallel approach and investigate various promising GT approaches (oligonucleotide chemistries, gene editing and gene delivery). Also, the consortium will engineer disease models for proper assessment of therapeutic interventions and aims to provide in vitro & in vivo preclinical proof-of-concept for the GT.
A significant benefit compared to current technologies is that the GT has the potential to be a curative treatment for rare cardiac diseases. Based on previous successes, GEREMY will target PLN & PKP2 as a roadmap of the technology. Restoring the primary defect in the PLN & PKP2 genes that cause the disease will lead to preserving or even restoring myocardial contractility. Through this approach, GEREMY will work towards a curative treatment of inherited ACM and likely other cardiomyopathies, which significantly reduces the healthcare burden.
The project’s experts in preclinical research and cardiac genetics will deliver preclinical efficacy and safety data for the mutation correction. The partners with regulatory and clinical trial expertise (EXOM, EUF, NLHI) will prepare for immediate start of clinical trials upon project completion, and apply for orphan drug designation. EUPATI, a patient organisation and KUL ethics partner will ensure that the project is continuously aligned with patient needs and ethical perspectives. The whole consortium will contribute to communicate an disseminate the results to ensure maximum exploitation of this breakthrough technology.

Campo scientifico (EuroSciVoc)

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HORIZON-RIA - HORIZON Research and Innovation Actions

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Coordinatore

STICHTING NETHERLANDS HEART INSTITUTE
Contributo netto dell'UE
€ 1 312 250,00
Costo totale
€ 1 312 250,00

Partecipanti (9)

Partner (1)