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

NCT02575430 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 59

Last updated 2016-04-29

No results posted yet for this study

Summary

To evaluate the natural history of visual function in subjects with IRD phenotypically diagnosed as Leber congenital amaurosis (LCA) or retinitis pigmentosa (RP) caused by RPE65 or LRAT gene mutations.

Conditions

  • Leber Congenital Amaurosis (LCA)
  • Retinitis Pigmentosa (RP)

Interventions

OTHER

No treatment: retrospective chart review

Sponsors & Collaborators

  • QLT Inc.

    lead INDUSTRY

Principal Investigators

  • David Saperstein, MD · QLT Inc.

Eligibility

Min Age
8 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-12-31
Primary Completion
2016-03-31
Completion
2016-03-31

Countries

  • United States
  • Canada
  • Denmark
  • Germany
  • Netherlands
  • Switzerland
  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02575430 on ClinicalTrials.gov