Natural History Study of Patients With Leber Congenital Amaurosis Associated With Mutations in RPE65

NCT02714816 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 37

Last updated 2023-08-14

No results posted yet for this study

Summary

MGT005 is a natural history study to collect longitudinal prospective data from patients with Leber Congenital Amaurosis associated with defects in RPE65.

Conditions

  • Leber Congenital Amaurosis

Sponsors & Collaborators

  • MeiraGTx UK II Ltd

    lead INDUSTRY

Principal Investigators

  • Michel Michealides, Prof · UCL/Moorfileds

Eligibility

Min Age
3 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-04-30
Primary Completion
2023-07-22
Completion
2023-07-22

Countries

  • United States
  • 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 NCT02714816 on ClinicalTrials.gov