drugset / Trial / NCT05848128

Efficacy and Safety Evaluation of Tavilermide Ophthalmic Solution for the Treatment of Dry Eye

NCT05848128 ↗

Phase 3 Completed 642 enrolled Mimetogen Pharmaceuticals USA, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of the study is to compare the efficacy and safety of 5% tavilermide ophthalmic solution to placebo for the treatment of the signs and symptoms of dry eye disease.

Timeline

Start
2023-06-28
Primary completion
2024-05-11
Completion
2024-05-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Tavilermide Protein / enzyme biologic 5 % Topical

Indications