CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 365 enrolled
Drug / intervention
REGN910-3 +1 moredrug
Likely dose
Not stated in 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/NCT02713204
NCT02713204Phase 2Completed

A Randomized, Double-Masked, Active-Controlled Phase 2 Study of the Efficacy, Safety, and Tolerability of Repeated Doses of Intravitreal REGN910-3 in Patients With Neovascular Age-Related Macular Degeneration

Regeneron Pharmaceuticals·interventional·Posted Mar 18, 2016·Updated May 7, 2019

In Brief

A Phase 2 clinical trial evaluating REGN910-3 and Intravitreal Aflibercept Injection (IAI) for Neovascular Age-Related Macular Degeneration. Completed, enrolled 365 participants across 87 sites.

Detailed Summary

The primary objective of the study is to compare the efficacy of intravitreal (IVT)-administered REGN910-3 compared to intravitreal aflibercept injection (IAI).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
20162017201820192020202120222023202420252026
First PostedMar 18, 2016
Enrollment StartMar 31, 2016
Primary CompletionOct 3, 2017
TodayJul 2, 2026
Enrollment to primary: 1.5 yearsPosted 10.3 years ago

Interventions

REGN910-3drug

Intravitreal Aflibercept Injection (IAI)drug