drugset / Trial / NCT00128245

Safety and Efficacy of Pimecrolimus Ophthalmic Suspension in Patients With Moderate to Severe Keratoconjunctivitis Sicca

NCT00128245

Phase 2 Completed 440 enrolled Novartis
RandomizedParallel-groupDouble-blindTreatment

Summary

This study evaluates the efficacy and safety of 2 doses of pimecrolimus (0.3% and 1%) ophthalmic suspension in a moderate to severe population of keratoconjunctivitis sicca (KCS, dry eye syndrome) patients.

Timeline

Start
2004-09
Primary completion
2006-12
Completion
2006-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Pimecrolimus Small molecule 0.3 %
Subject Pimecrolimus Small molecule 1 %

Indications