A Phase 3 Safety and Efficacy Study of Fovista® (E10030) Intravitreous Administration in Combination With Lucentis® Compared to Lucentis® Monotherapy
Clinical trial NCT01944839 · TERMINATED
Trial details
- NCT number
- NCT01944839
- Sponsor
- Ophthotech Corporation
- Status
- TERMINATED
- Phase
- Phase 3
- Study type
- INTERVENTIONAL
- Start date
- 2013-08-01
- Primary completion
- 2016-12-01
- Enrollment
- 619
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