drugset / Trial / NCT00725686

Study of PF-04523655 (REDD14NP) In Subjects With Choroidal Neovascularization (CNV) Secondary to Age-Related Macular Degeneration (Wet AMD)

NCT00725686

Phase 1 Completed 54 enrolled Quark Pharmaceuticals Pfizer · collab
NaSingle-groupOpen-labelTreatment

Summary

The aim of the study is to evaluate whether PF-04523655 is safe in the treatment of neovascular/wet AMD

Timeline

Start
2007-02
Primary completion
2010-11
Completion
2010-11

Drugs

EvaluationDrugModalityDoseRoute
Subject PF-04523655 Small interfering RNA (siRNA) 50 ug Intravitreal
Subject PF-04523655 Small interfering RNA (siRNA) 100 ug Intravitreal
Subject PF-04523655 Small interfering RNA (siRNA) 200 ug Intravitreal
Subject PF-04523655 Small interfering RNA (siRNA) 400 ug Intravitreal
Subject PF-04523655 Small interfering RNA (siRNA) 670 ug Intravitreal
Subject PF-04523655 Small interfering RNA (siRNA) 1000 ug Intravitreal
Subject PF-04523655 Small interfering RNA (siRNA) 1500 ug Intravitreal
Subject PF-04523655 Small interfering RNA (siRNA) 2250 ug Intravitreal
Subject PF-04523655 Small interfering RNA (siRNA) 3000 ug Intravitreal