drugset / Trial / NCT03622580

A Study to Evaluate the Efficacy and Safety of Faricimab (RO6867461) in Participants With Diabetic Macular Edema (YOSEMITE)

NCT03622580 ↗

Phase 3 Completed 940 enrolled Hoffmann-La Roche
RandomizedParallel-groupTriple-blindTreatment

Summary

This study will evaluate the efficacy, safety, and pharmacokinetics of faricimab administered at 8-week intervals or as specified in the protocol following treatment initiation, compared with aflibercept once every 8 weeks (Q8W), in participants with diabetic macular edema (DME).

Timeline

Start
2018-09-05
Primary completion
2020-10-20
Completion
2021-09-03

Outcome

Met primary endpoint

paper Non-inferiority for the primary endpoint was achieved with faricimab every 8 weeks PMID 35085503 ↗

release “Both studies met their primary endpoint with faricimab consistently shown to offer non-inferior visual acuity gains to aflibercept.” gene.com ↗

release “YOSEMITE and RHINE studies Roche's faricimab meets primary endpoint and shows strong durability across two global phase III studies for diabetic macular edema” chugai-pharm.co.jp ↗

Publications

Drugs

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