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The project in the news

​Fibroblast activation and abnormal extracellular matrix remodelling as common hallmarks in three cancer-prone genodermatoses

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Clinically-relevant correction of Recessive Dystrophic Epidermolysis Bullosa by dual sgRNA CRISPR/Cas9-mediated gene editing

     

 

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Designación de medicamento huérfano: Autologous skin equivalent graft composed of keratinocytes and fibroblasts genetically corrected by CRISPR/Cas9-mediated excision of mutation-carrying COL7A1 exon 80.

Indicación: Tratamiento de la epidermólisis bullosa

PROMOTOR: CIBERER

ENTIDADES PARTICIPANTES: CIEMAT (25%), CIBERER (30%), UC3M (33%), CCST (2%), FJD (10%)

Inventores: F Larcher, R Murillas, A Mencia, J Bonafont, MJ Escámez, A Meana, SG Llames, S Modamio, MC de Arriba, L Martínez, M García, M del Río,

Aceptación EMA: 28/02/2020.

Referencia: EMA/OD/0000013899

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News for EB Patients and Professionals

 

DEBRA-Spain
The DEBRA- Butterfly Skin Association is a national reference in Epidermolysis bullosa that has the declaration of Public Utility issued by the Ministry of the Interior.

 

EB-Research Network

The International Clinical Network of EB Centers and Experts promotes the exchange of EB knowledge and experience to ensure professional treatment for patients and a simplification of cross-border medical care as well as to create a basis for future clinical studies for the treatment of EB .

 

ORPHANET

The portal on rare diseases and orphan drugs that gathers and improves knowledge to improve the diagnosis, care and treatment of people who suffer from them.

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