NCT02575430View on ClinicalTrials.gov

Natural History Study in Inherited Retinal Disease Subjects Caused by Mutations in RPE65 or LRAT

CompletedOBSERVATIONAL
Enrollment

59

Participants

Timeline

Start Date

December 31, 2015

Primary Completion Date

March 31, 2016

Study Completion Date

March 31, 2016

Conditions
Leber Congenital Amaurosis (LCA)Retinitis Pigmentosa (RP)
Interventions
OTHER

No treatment: retrospective chart review

Trial Locations (9)

21287

Wilmer Eye Institute - Johns Hopkins Hospital, Baltimore

72076

STZ Eyetrial at the Department of Ophthalmology - University of Tübingen, Tübingen

97239-4197

Casey Eye Institute - Marquam Hill, Portland

M5G 1X8

The Hospital for Sick Children, Ophthalmology and Vision Sciences, Toronto

H4A 3J1

Montreal Children's Hospital, McGill University Health Centre, Montreal

Unknown

Glostrup Hospital and National Eye Clinic at the Kennedy Center, Glostrup Municipality

3011 BH

Rotterdam Ophthalmic Institute, Rotterdam

CH-1004

Jules Gonin Eye Hospital - Oculogenetic Unit, Lausanne

EC1V 2PD

Moorfields Eye Hospital - Research and Treatment Centre, London

All Listed Sponsors
lead

QLT Inc.

INDUSTRY

NCT02575430 - Natural History Study in Inherited Retinal Disease Subjects Caused by Mutations in RPE65 or LRAT | Biotech Hunter | Biotech Hunter