drugset / Trial / NCT01027650
Safety and Efficacy of AGN208397 in the Treatment of Macular Edema Associated With Retinal Vein Occlusion (RVO)
RandomizedParallel-groupDouble-blindTreatment
Summary
This study will evaluate the safety and efficacy of a single intravitreal injection of AGN208397 to treat Macular Edema associated with Retinal Vein Occlusion. This study is being conducted in two stages: Stage 1 will enroll approximately 21 subjects who will receive a single open label intravitreal injection of either 75 ug, 300 ug, 600 ug or 900 ug of AGN208397 and be followed for 12 months post treatment; based on Stage 1 results, Stage 2 will enroll approximately 96 subjects who will receive a single masked intravitreal injection of one of three doses of AGN208397 or Ozurdex® and be followed for 12 months post treatment.
Timeline
- Start
- 2010-03
- Primary completion
- 2012-04
- Completion
- 2013-02
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | AGN208397 | Unknown | 75 ug | Intravitreal |
| Subject | AGN208397 | Unknown | 300 ug | Intravitreal |
| Subject | AGN208397 | Unknown | 450 ug | Intravitreal |
| Subject | AGN208397 | Unknown | 600 ug | Intravitreal |
| Subject | AGN208397 | Unknown | 900 ug | Intravitreal |
| Comparator | Dexamethasone | Small molecule | 700 ug | Intravitreal |