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Oral QLT091001 in Retinitis Pigmentosa (RP) Subjects With an Autosomal Dominant Mutation in Retinal Pigment Epithelial 65 Protein (RPE65)

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Clinical Trial

RET RP 01 - NCT01543906 Completed
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 DominantMutation in Retinal Pigment Epithelial 65 Protein (RPE65).

Phase 1
Interventional

Disease

Disease type

Retinitis Pigmentosa

Orphan drug recognition

No

Patient type

Adult

Children

Inclusion / Exclusion

Opening date

01/02/2012

Closing date

01/07/2014

Inclusion criteria :

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Exclusion criteria :

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Funding

industry

Members involved

Main investigators

Dr David KEEGAN

Representative

Ireland

Working Group Leader
See more

ERN EYE member investigating site

HCP : Principal investigators