drugset / Trial / NCT02434328

Efficacy and Safety of RTH258 Versus Aflibercept - Study 2

NCT02434328 ↗

Phase 3 Completed 1048 enrolled Alcon Research
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to compare brolucizumab (RTH258) ophthalmic solution for intravitreal (IVT) injection (6 mg) to aflibercept ophthalmic solution for IVT injection (2 mg) in subjects with untreated active choroidal neovascularization (CNV) secondary to age-related macular degeneration (AMD) in the study eye.

Timeline

Start
2015-07-28
Primary completion
2017-04-05
Completion
2018-03-08

Outcome

Met primary endpoint

registry analysis (non-inferiority test); Brolucizumab 6 mg vs Aflibercept 2 mg; p <0.0001; Least Squares Mean Difference -0.7 (95% CI -2.4 to 1.0) NCT02434328 ↗

paper Brolucizumab was noninferior to aflibercept in visual function at Week 48 PMID 30986442 ↗

release “As previously announced, HAWK and HARRIER met their primary endpoint of non-inferiority in mean change in BCVA at week 48 with brolucizumab versus aflibercept” novartis.com ↗

release “The EC approval was based on findings from the Phase III HAWK and HARRIER clinical trials, in which Beovu met the primary endpoint,” novartis.com ↗

Drugs

EvaluationDrugModalityDoseRoute
Comparator Aflibercept Protein / enzyme biologic 2 mg Intravitreal
Subject Brolucizumab Other / unclassified 6 mg Intravitreal