drugset / Trial / NCT02511613

Effect of Squalamine Lactate Ophthalmic Solution, 0.2% in Subjects With Neovascular Age-Related Macular Degeneration

NCT02511613

Phase 2 Withdrawn Ohr Pharmaceutical Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to evaluate anatomical and functional effect of combination therapy of Squalamine Lactate Ophthalmic Solution, 0.2% administered twice daily with monthly ranibizumab intravitreal injections in patients with choroidal neovascularization due to AMD.

Timeline

Start
2015-07
Primary completion
2016-04
Completion
2016-04

Drugs

EvaluationDrugModalityDoseRoute
Comparator Squalamine Unknown 0.2 % Topical
Comparator Ranibizumab Monoclonal antibody Intravitreal