drugset / Trial / NCT00722384

Open Label Study for the Evaluation of Tolerability of Five Dose Levels of Cand5

NCT00722384

Phase 1 Completed 15 enrolled OPKO Health, Inc.
Non-randomizedParallel-groupOpen-labelTreatment

Summary

To establish the tolerability and preliminary efficacy of Cand5 by a single intravitreal injection in patients with wet age-related macular degeneration.

Timeline

Start
2004-08
Primary completion
2007-08
Completion
2007-12

Drugs

EvaluationDrugModalityDoseRoute
Subject bevasiranib Unknown 0.1 mg Intravitreal
Subject bevasiranib Unknown 0.33 mg Intravitreal
Subject bevasiranib Unknown 1 mg Intravitreal
Subject bevasiranib Unknown 1.5 mg Intravitreal
Subject bevasiranib Unknown 3 mg Intravitreal

Indications