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Santen 32-009

Status: Ongoing, but not recruiting participants Identifier: NCT02251938

Santen 32-009: A Phase IIIB, Multi-National, Multi-Center, Open-Label Extension Study Assessing the long-term Safety of the PRN Intravitreal Injections of DE-109 in subjects with Non-Infectious Uveitis of the Posterior Segment of the Eye who have participated in the SAKURA Development program.

Condition: Non-Infectious Uveitis of the Posterior Segment of the Eye

Study Type: Interventional

Duration: 12 months


  • Ages: 18 years and older
  • Sexes: All
  • Accepts Healthy Volunteers: No

For additional information on this study, please click here

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