drugset / Trial / NCT01577381

Efficacy, Safety And Tolerability Study Of RN6G In Subjects With Geographic Atrophy Secondary to Age-related Macular Degeneration

NCT01577381 ↗

Phase 2 Terminated 10 enrolled Pfizer
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to determine the efficacy, safety and tolerability of multiple doses of RN6G in subjects with Geographic Atrophy Secondary to Age-related Macular Degeneration.

Timeline

Start
2012-08
Primary completion
2013-09
Completion
2013-10

Outcome

Outcome not reported

Stopped: “See termination reason in detailed description.”

Drugs

EvaluationDrugModalityDoseRoute
Subject RN6G Unknown 2.5 mg/kg Intravenous
Subject RN6G Unknown 15 mg/kg Intravenous