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Clinical Trial Summary

The objective of the study is to evaluate the efficacy and safety of two different treatment regimens of EYS606.


Clinical Trial Description

This is a Phase 2, multi-center, randomized open-label interventional study of EYS606 in subjects with active chronic non-infectious uveitis. The maximum study duration per patient is 51 Weeks (including an up to 3 week screening period + 48 weeks follow-up after treatment). The study will be conducted in 2 parts. Part I is a safety cohort phase that will enroll up to 6 subjects, Part II is the randomized comparison phase that will enroll up to an additional 50 subjects. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04207983
Study type Interventional
Source Eyevensys
Contact
Status Completed
Phase Phase 2
Start date February 3, 2020
Completion date October 5, 2021

See also
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