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Clinical Trial Summary

The purpose of this study is to evaluate the safety and tolerability of QR-110 administered via intravitreal injection in subjects with LCA due to the CEP290 p.Cys998X mutation.


Clinical Trial Description

The purpose of this study is to evaluate the safety and tolerability of QR-110 administered via intravitreal injection in subjects with LCA due to the CEP290 p.Cys998X mutation. Subjects will receive QR-110 in one eye every 3 months, for a maximum of 4 doses. Up to 3 dose levels of QR-110 will be evaluated. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03140969
Study type Interventional
Source ProQR Therapeutics
Contact
Status Completed
Phase Phase 1/Phase 2
Start date October 16, 2017
Completion date October 2, 2019