drugset / Trial / NCT00891735

A Study of Ranibizumab Administered Monthly or on an As-needed Basis in Patients With Subfoveal Neovascular Age-related Macular Degeneration (HARBOR)

NCT00891735 ↗

Phase 3 Completed 1097 enrolled Genentech, Inc.
RandomizedParallel-groupTriple-blindTreatment

Summary

This is a Phase III, multicenter, randomized, double-masked, dose-comparison study of the efficacy and safety of ranibizumab injection administered intravitreally to patients with choroidal neovascularization (CNV) secondary to age-related macular degeneration (AMD). Results are presented for the first 12 months of the study.

Timeline

Start
2009-07
Primary completion
2011-08
Completion
2012-08

Outcome

Missed primary endpoint

paper At month 12, the ranibizumab 2.0 mg monthly group did not meet the prespecified superiority comparison PMID 23352196 ↗

paper the ranibizumab 0.5 mg and 2.0 mg PRN groups did not meet the prespecified noninferiority (NI) comparison PMID 23352196 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Ranibizumab Monoclonal antibody 0.5 mg Intravitreal
Subject Ranibizumab Monoclonal antibody 2 mg Intravitreal