Projekt
Gene Therapy for treatment of rare inherited Arrhythmogenic Cardiomyopathy
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) fo…
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.
Themengebiete
- Gesundheit Gesundheit – Überblick über Forschungsprojekte, Patente und Akteure im TechnologieAtlas.
Hochschulen
- STICHTING NETHERLANDS HEART INSTITUTE STICHTING NETHERLANDS HEART INSTITUTE – Hochschule bzw. Forschungseinrichtung mit Aktivitäten in Forschung un…
- KONINKLIJKE NEDERLANDSE AKADEMIE VAN WETENSCHAPPEN - KNAW KONINKLIJKE NEDERLANDSE AKADEMIE VAN WETENSCHAPPEN - KNAW – Hochschule bzw. Forschungseinrichtung mit Aktivit…
- FUNDACAO GIMM - GULBENKIAN INSTITUTE FOR MOLECULAR MEDICINE FUNDACAO GIMM - GULBENKIAN INSTITUTE FOR MOLECULAR MEDICINE – Hochschule bzw. Forschungseinrichtung mit Aktiv…
- KLINIKUM DER TECHNISCHEN UNIVERSITÄT MÜNCHEN (TUM KLINIKUM) KLINIKUM DER TECHNISCHEN UNIVERSITÄT MÜNCHEN (TUM KLINIKUM) – Hochschule bzw. Forschungseinrichtung mit Aktiv…
- KATHOLIEKE UNIVERSITEIT LEUVEN KATHOLIEKE UNIVERSITEIT LEUVEN – Hochschule bzw. Forschungseinrichtung mit Aktivitäten in Forschung und Innov…
- King's College London King's College London – Hochschule bzw. Forschungseinrichtung mit Aktivitäten in Forschung und Innovation.
Unternehmen
- EXOM DEUTSCHLAND GMBH EXOM DEUTSCHLAND GMBH – Unternehmen mit Aktivitäten in Forschung und Innovation.