Gene therapy (AAV vector) · developed by ProQR Therapeutics
QR-1123 is an AAV gene therapy in development for autosomal dominant retinitis pigmentosa and other inherited retinal dystrophies.
Summary written with AI from the sources listed at the end of this page.
| Trial | Phase | Condition | Status | Sponsor |
|---|---|---|---|---|
| NCT04123626 | Phase 1/2 | Autosomal Dominant Retinitis Pigmentosa | Active not recruiting | PRQR |
Trials of the companies BioRadar tracks, from ClinicalTrials.gov, most advanced phase first.
Autosomal Dominant Retinitis PigmentosaEye DiseasesEye Diseases, HereditaryRetinal DiseaseRetinal DystrophiesRetinitisVision DisordersVision Tunnel
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