drugset / Trial / NCT01915940

Bimatoprost Ocular Insert Compared to Topical Timolol Solution in Patients With Glaucoma or Ocular Hypertension

NCT01915940

Phase 2 Completed 169 enrolled ForSight Vision5, Inc.
RandomizedParallel-groupTriple-blindTreatment

Summary

The objective of this Phase 2 study is to evaluate whether the Bimatoprost Ocular Insert is non-inferior to that of timolol ophthalmic solution (0.5%) at 12 weeks.

Timeline

Start
2013-10-23
Primary completion
2014-09-30
Completion
2014-11-14

Drugs

EvaluationDrugModalityDoseRoute
Subject Bimatoprost Other / unclassified 13 mg Other
Comparator Timolol Other / unclassified 0.5 % Topical