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Clinical Trial Summary

This is a phase I/II randomized, masked, clinical trial to determine the safety and efficacy of intravitreal administration of cerliponase alfa.


Clinical Trial Description

This is a Phase I/II study for 5 subjects receiving an intravitreal injection of cerliponase alfa under sedation into the proclaimed study eye(s) in a 4-week interval over 24 months. This study will be monitored by a Data Safety Monitoring Committee (DSMB). Each subject will participate in the ongoing study for an active period of 2 years. Subjects will then transfer to a bi-annual monitoring program where data will be collected from bi-annual standard of care visits for an additional 3 years. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05152914
Study type Interventional
Source Nationwide Children's Hospital
Contact
Status Active, not recruiting
Phase Phase 1/Phase 2
Start date November 1, 2021
Completion date November 1, 2027