drugset / Trial / NCT02039765

Pharmacokinetics and Safety of Topical Administration of Brimonidine Tartrate Ophthalmic Solution 0.025%.

NCT02039765

Phase 1 Completed 12 enrolled Bausch & Lomb Incorporated ORA, Inc. · collab
NaSingle-groupOpen-labelScreening

Summary

To characterize the plasma pharmacokinetics and safety profile of brimonidine following a single dose and 4 times per day (QID) dosing of brimonidine tartrate ophthalmic solution 0.025% for 7 days in healthy, adult subjects.

Timeline

Start
2014-02
Primary completion
2014-03
Completion
2014-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Brimonidine Small molecule 0.025 % Topical

Indications