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Efficacy and safety of QLT091001 in subjects with Inherited Retinal Disease (IRD) caused by gene mutations.
Status of the trial: Unknown
Orphan Drug Recognition: No
- Opening Date: 2017-12-12
- Closing Date: 2018-12-12
Inclusion: Genotype-confirmed Leber congenital amaurosis attributable
Exclusion: Prior gene therapy
Funder Type: industry
HCP: Principal investigators
HCP: Other investigators
Within ERN-EYE members
- Retinal Rare Eye Diseases (WG1)
This ERN is supported by:
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