Clinical trial
A First-in-Human Study to Evaluate the Safety and Tolerability of QR-421a in Subjects With Retinitis Pigmentosa (RP) Due to Mutations in Exon 13 of the USH2A Gene
NCT03780257 is registered in ClinicalTrials.gov with ProQR Therapeutics as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A First-in-Human Study to Evaluate the Safety and Tolerability of QR-421a in Subjects With Retinitis Pigmentosa (RP) Due to Mutations in Exon 13 of the USH2A Gene
- Lead sponsor
- ProQR Therapeutics
- Phase
- Phase 1/2
- Overall status
- Completed
- Start date
- March 6, 2019
- Completion date
- October 14, 2021
- Enrollment
- 20 (actual)
- Sites
- 7
Conditions
As the registry lists them; a condition with its own page is linked.
deaf blind, eye diseases, eye diseases, hereditary, eye disorders congenital, retinal disease, retinitis pigmentosa, usher syndrome type 2, vision disorders