University Medical Center Utrecht at ESGCT 2026
Oct 27–30, 2026 Hamburg, Germany ~2.5k attendees Website
University Medical Center Utrecht brings 8 presentations to ESGCT 2026 in Hamburg. Its work centres on base and prime editing in models of inherited metabolic, liver and lung disease, including primary ciliary dyskinesia and galactosemia. Other strands cover scalable in vivo editing of blood stem cells and market access for these therapies.
| Organization | ESGCT 2026 Attendance |
|---|---|
University Medical Center Utrecht Utrecht, Netherlands | |
Dutch academic hospital whose regenerative medicine centre models genetic diseases with gene editing. | Talk Wed Oct 28 9:45am–10:30am NEO-AAV: an engineered extracellular vesicle-enveloped AAV platform for activation-coupled T cell transduction and CAR-T cell generation Vectors and delivery (AAV, lentiviral, LNP)Cell therapies and CAR-T Poster Wed Oct 28 1:30pm–3:30pm Precision adenine base editing of a pathogenic OTC variant in engineered hepatic models Talk Thu Oct 29 9:50am–10:30am Challenges in market access of GCTs Manufacturing, CMC and access Poster Thu Oct 29 2:00pm–4:00pm Antibody-based targeted lysosomal degradation of circulating amyloidogenic immunoglobulin light chains as a novel therapeutic strategy for AL amyloidosis Poster Thu Oct 29 2:00pm–4:00pm Less Is More: Defining healthy cell thresholds to restore mucociliary clearance in Primary Ciliary Dyskinesia Rare and inherited disease Poster Thu Oct 29 2:00pm–4:00pm Mismatched pegRNAs to inhibit self-complementarity of PBS and spacer for Classic Galactosemia Poster Thu Oct 29 2:00pm–4:00pm Toward scalable in vivo HSC genome editing for mevalonate kinase deficiency and beyond: a platform-based preclinical approach Talk Fri Oct 30 10:15am–10:30am Back to the Bases: Scalable Modeling of Primary Ciliary Dyskinesia Variants with Base Editing Gene and epigenome editingRare and inherited disease |
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