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RET RP 01 - NCT01543906
Oral QLT091001 in Retinitis Pigmentosa (RP) Subjects With an Autosomal Dominant Mutation in Retinal Pigment Epithelial 65 Protein (RPE65)
Oral QLT091001 in Retinitis Pigmentosa (RP) Subjects With an Autosomal Dominant
Mutation in Retinal Pigment Epithelial 65 Protein (RPE65).
Type: Interventional
Status of the trial: Completed
Orphan Drug Recognition: No
Inclusion
- Opening Date: 2012-02-01
- Closing Date: 2014-07-01
Criteria
Children: No
Adults: Yes
Funder Type: industry
HCP: Principal investigators
HCP: Other investigators
Within ERN-EYE members
Workgroups
Retinal Rare Eye Diseases (WG1)