drugset / Trial / NCT01229215

A Study of Safety, Tolerability, and Evidence of Activity of FCFD4514S Administered Monthly or Every Other Month to Patients With Geographic Atrophy

NCT01229215 ↗

Phase 2 Completed 143 enrolled Genentech, Inc.
RandomizedParallel-groupSingle-blindTreatment

Summary

This is a Phase Ib/II, multicenter, randomized, single-masked, sham-injection-controlled study of safety, tolerability, and evidence of activity of FCFD4514S intravitreal injections administered monthly or every other month in patients with geographic atrophy.

Timeline

Start
2011-02
Primary completion
2013-04
Completion
2013-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Lampalizumab Monoclonal antibody — Intravitreal