E10030
Sponsors
Ophthotech Corporation, National Eye Institute (NEI)
Conditions
Age-Related Macular DegenerationAge-related Macular DegenerationVon Hippel-Lindau Syndrome
Phase 1
A Phase 1, Safety, Tolerability and Pharmacokinetic Profile of Intravitreous Injections of E10030 (Anti-PDGF Pegylated Aptamer) in Subjects With Neovascular Age-Related Macular Degeneration
CompletedNCT00569140
Start: 2007-12-31End: 2008-12-31Target: 18Updated: 2024-02-21
A Phase I/II Trial for Intravitreous Treatment of Severe Ocular Von Hippel-Lindau Disease Using a Combination of the PDGF Antagonist E10030 and the VEGF Antagonist Ranibizumab
CompletedNCT02859441
Start: 2017-01-23End: 2019-07-09Updated: 2021-11-01
Phase 3
A Phase 3 Safety and Efficacy Study of Fovista® (E10030) Intravitreous Administration in Combination With Either Avastin® or Eylea® Compared to Avastin® or Eylea® Monotherapy
TerminatedNCT01940887
Start: 2014-05-31End: 2017-09-30Updated: 2024-10-31
A Phase 3 Safety and Efficacy Study of Fovista® (E10030) Intravitreous Administration in Combination With Lucentis® Compared to Lucentis® Monotherapy
TerminatedNCT01940900
Start: 2013-08-31End: 2016-12-31Updated: 2024-10-30
A Phase 3 Safety and Efficacy Study of Fovista® (E10030) Intravitreous Administration in Combination With Lucentis® Compared to Lucentis® Monotherapy
TerminatedNCT01944839
Start: 2013-08-31End: 2016-12-31Updated: 2024-10-30