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Clinical trial

A Phase 3 Randomized, Double-masked, Controlled Trial to Establish the Safety and Efficacy of Intravitreous Administration of Fovista® (Anti PDGF-B Pegylated Aptamer) Administered in Combination With Lucentis® Compared to Lucentis® Monotherapy in Subjects With Subfoveal Neovascular Age-related Macular Degeneration.

NCT01940900 is registered in ClinicalTrials.gov with Ophthotech Corporation as lead sponsor.

NCT NCT01940900
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Registry record

As filed in ClinicalTrials.gov.

Title
A Phase 3 Randomized, Double-masked, Controlled Trial to Establish the Safety and Efficacy of Intravitreous Administration of Fovista® (Anti PDGF-B Pegylated Aptamer) Administered in Combination With Lucentis® Compared to Lucentis® Monotherapy in Subjects With Subfoveal Neovascular Age-related Macular Degeneration.
Lead sponsor
Ophthotech Corporation
Phase
Phase 3
Overall status
Terminated
Start date
August 31, 2013
Completion date
December 31, 2016
Enrollment
627 (actual)
Sites
121

Conditions

As the registry lists them; a condition with its own page is linked.

age-related macular degeneration