drugset / Trial / NCT02242032

Study of the Safety and Tolerability of P 321 Ophthalmic Solution in Subjects With Dry Eye Disease

NCT02242032 ↗

Phase 1 Completed 53 enrolled Parion Sciences
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to assess the safety and tolerability of P-321 Ophthalmic Solution in subjects with mild to moderate dry eye disease.

Timeline

Start
2014-07
Primary completion
2015-03
Completion
2015-03

Drugs

EvaluationDrugModalityDoseRoute
Subject P-321 Unknown 0.0005 % Other
Subject P-321 Unknown 0.0015 % Other
Subject P-321 Unknown 0.005 % Other
Subject P-321 Unknown 0.01 % Other

Indications