
Project objective:
Development of an innovative therapy for cystic fibrosis using advanced technologies based on extracellular vesicles and genome editing tools(CRISPR/Cas9).
Planned tasks:
- Correction of the CFTR gene responsible for disease onset in a lung epithelial cell line
- Amelioration of pulmonary fibrosis symptoms in a mouse model
- Attempt to achieve correction of the CFTR gene in experimental animals
- Purchase of research equipment: hypoxic incubator, automatic vesicle fraction collector, FlowJo software
Target groups:
- Cystic fibrosis patients
- Patients affected by fibrotic diseases
- Scientists working in the field of biomedical sciences
- Technology recipients: companies in the biopharmaceutical industry interested in implementing new drug candidates
Project value: 3,912,680.00 PLN (ca. € 912,000)
EU funding: 3,912,680.00 PLN (ca. € 912,000)
Principal investigator:
Sylwia Bobis-Wozowicz, PhD (Jagiellonian University)
Scientific Partner:
Prof. Toni Cathomen (Director of the Institute of Transfusion Medicine and Gene Therapy, Medical Center – University of Freiburg, Germany)
Business Partner:
Xenstats, CEO: Prof. Aneta Sawikowska (Poznań, Poland)