drugset / Trial / NCT04740905

A Study to Evaluate the Efficacy and Safety of Faricimab in Participants With Macular Edema Secondary to Branch Retinal Vein Occlusion

NCT04740905 ↗

Phase 3 Completed 553 enrolled Hoffmann-La Roche Chugai Pharmaceutical · collab
RandomizedParallel-groupTriple-blindTreatment

Summary

This is a Phase III, multicenter, randomized, double-masked, active comparator-controlled, parallel-group study evaluating the efficacy, safety, and pharmacokinetics of faricimab administered by intravitreal (IVT) injection at 4-week intervals until Week 24, followed by a double-masked period of study without active control to evaluate faricimab administered according to a personalized treatment interval (PTI) dosing regimen in participants with macular edema due to branch retinal vein occlusion (BRVO).

Timeline

Start
2021-03-02
Primary completion
2022-07-06
Completion
2023-06-12

Outcome

Met primary endpoint

paper The BCVA gains from the baseline to week 24 with faricimab were noninferior versus aflibercept in BALATON PMID 38280653 ↗

release “Both studies met their primary endpoint, with Vabysmo showing non-inferior visual acuity gains compared to aflibercept.” gene.com ↗

release “Vabysmo met its primary endpoint in two clinical trials, BALATON and COMINO” roche.com ↗

Drugs

EvaluationDrugModalityDoseRoute
Comparator Aflibercept Protein / enzyme biologic 2 mg Intravitreal
Subject Faricimab Monoclonal antibody 6 mg Intravitreal