Maximum tolerated dose of a humanized anti-vascular endothelial growth factor antibody fragment for treating neovascular age-related macular degeneration

Philip J. Rosenfeld, Steven D. Schwartz, Mark S. Blumenkranz, Joan W. Miller, Julia A. Haller, James D. Reimann, William L. Greene, Naveed Shams

Research output: Contribution to journalArticle

205 Scopus citations

Abstract

Purpose: To investigate the maximum tolerated dose of ranibizumab administered as a single intravitreal injection. Design: Open-label, 5-center, uncontrolled, prospective, dose-ranging, interventional case series. Participants: Twenty-seven patients with subfoveal choroidal neovascularization (CNV) secondary to age-related macular degeneration (AMD) with best-corrected Snellen equivalent visual acuity (VA) of 20/100 or worse and considered ineligible for laser photocoagulation or photodynamic therapy. Methods: A single intravitreal injection of ranibizumab was to be administered at 1 of 6 escalating doses (50, 150, 300, 500, 1000, and 2000 μg), with escalation to the next dose level occurring only after the safety and tolerability of the lower dose level was established through postinjection day 14. Follow-up examinations were performed on postinjection days 1, 3, 7, 14, 42, and 90. Enrollment was stopped if <2 patients experienced dose-limiting toxicity. Main Outcome Measures: The primary safety measures were changes from baseline in VA, intraocular pressure (IOP), intraocular inflammation, and production of antiranibizumab antibody. Dose-limiting toxicity was defined by intraocular inflammation, elevated IOP, reduced VA, or hemorrhage within 90 days after injection. Results: All patients completed this single intravitreal injection study, and 500 μg of ranibizumab was the maximum tolerated dose. At the higher dose of 1000 μg, significant intraocular inflammation was noted. All adverse events were self-limited, and no infectious endophthalmitis occurred. Aqueous or vitreous ocular inflammation occurred in 12 subjects, with complete resolution within 42 days. In 9 of the subjects, the inflammation was graded as trace to 1+ and required no treatment; in 3 of the subjects, the inflammation was graded as 2+ or 3+, and 2 of the 3 were treated with topical 1% prednisolone acetate. No serum antiranibizumab antibodies were detected. All patients had VA similar or improved compared with baseline values. Conclusion: The maximum tolerated single dose of ranibizumab in neovascular AMD patients was 500 μg. Single intravitreal injections of ranibizumab up to a dose of 500 μg were safe and well tolerated in this small group of patients.

Original languageEnglish (US)
Pages (from-to)1048-1053.e4
JournalOphthalmology
Volume112
Issue number6
DOIs
StatePublished - Jun 2005

ASJC Scopus subject areas

  • Ophthalmology

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