CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 1,217 enrolled
Drug / intervention
ranibizumab +3 morebiological
Likely dose
ranibizumab 0.5mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00509795
NCT00509795Phase 3Completed

A Randomized, Double Masked, Active Controlled Phase III Study of the Efficacy, Safety, and Tolerability of Repeated Doses of Intravitreal VEGF Trap in Subjects With Neovascular Age-Related Macular Degeneration

Regeneron Pharmaceuticals·interventional·Posted Aug 1, 2007·Updated Dec 28, 2012

In Brief

A Phase 3 clinical trial evaluating ranibizumab and aflibercept injection (VEGF Trap-Eye, BAY86-5321) for Macular Degeneration. Completed, enrolled 1,217 participants across 188 sites in 2 countries.

Detailed Summary

This study is a phase 3, double-masked, randomized, study of the efficacy and safety of VEGF Trap-Eye in patients with neovascular age-related macular degeneration. Approximately 1200 patients will be randomized in the US and Canada.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesCanada, United States
CollaboratorsBayer

Timeline

Phase 3CompletedFinished
20082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedAug 1, 2007
Enrollment StartAug 1, 2007
Primary CompletionSep 1, 2010
Study CompletionJul 1, 2011
TodayJul 2, 2026
Enrollment to primary: 3.1 yearsPosted 18.9 years ago

Interventions

ranibizumabbiological

Participants received a 0.5mg dose of ranibizumab via intravitreal (IVT) injection every 4 weeks for the first year. Thereafter a dose may be administered as frequently as every 4 weeks, but no less frequently than every 12 weeks.

aflibercept injection (VEGF Trap-Eye, BAY86-5321)biological

Participants received a 2.0mg dose of aflibercept injection every 4 weeks for the first year. Thereafter a dose may be administered as frequently as every 4 weeks, but no less frequently than every 12 weeks.

aflibercept injection (VEGF Trap-Eye, BAY86-5321)biological

Participants received a 0.5mg dose of aflibercept injection every 4 weeks for the first year. Thereafter a dose may be administered as frequently as every 4 weeks, but no less frequently than every 12 weeks.

aflibercept injection (VEGF Trap-Eye, BAY86-5321)biological

Participants received a 2.0mg dose of aflibercept injection every 8 weeks (including one additional 2.0 mg dose at Week 4) for the first year and were to receive sham injections at interim monthly visits. Thereafter a dose may be administered as frequently as every 4 weeks, but no less frequently than every 12 weeks.