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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