Observational Study to Assess the Effect of Iluvien® in DME Patients Insufficiently Responsive to Available Therapies
NCT02080091 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 25
Last updated 2015-08-26
Summary
This observational study aims to assess the safety and effect of Iluvien® in DME patients considered insufficiently responsive to available therapies in a real life setting in Germany.
Conditions
- Diabetic Macular Edema (DME)
Sponsors & Collaborators
-
Alimera Sciences
lead INDUSTRY
Principal Investigators
-
Professor Helmut Hoeh, MD · Dietrich-Bonhoeffer-Klinikum
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2013-12-31
- Primary Completion
- 2015-03-31
- Completion
- 2015-04-30
Countries
- Germany
Study Locations
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