drugset / Trial / NCT00877032

Safety And Tolerability Study Of RN6G In Patients With Dry, Age-Related Macular Degeneration

NCT00877032 ↗

Phase 1 Completed 57 enrolled Pfizer
RandomizedSingle-groupQuadruple-blindPrevention

Summary

The purpose of this study is to determine the safety and tolerability of RN6G in patients with dry, age-related macular degeneration.

Timeline

Start
2009-04
Primary completion
2011-07
Completion
2011-07

Drugs

EvaluationDrugModalityDoseRoute
Subject RN6G Unknown 0.3 mg/kg Intravenous
Subject RN6G Unknown 40 mg/kg Intravenous