A 48 Week Study to Evaluate the Efficacy and Safety of Two (2) EYS606 Treatment Regimens in Subjects With Active Chronic Non-infectious Uveitis (CNIU)

  • End date
    Jun 24, 2022
  • participants needed
  • sponsor
Updated on 24 January 2021


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


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.

Condition Non Infectious Uveitis
Treatment EYS606
Clinical Study IdentifierNCT04207983
Last Modified on24 January 2021


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