drugset / Trial / NCT05695781

Assessment of the Safety and Efficacy of BRM421 Ophthalmic Solutions in Dry Eye Subjects.

NCT05695781 ↗

Phase 3 Completed 740 enrolled BRIM Biotechnology Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

The objective of this study is to compare the safety and efficacy of BRM421 OS to vehicle for the treatment of the signs and symptoms of dry eye disease.

Timeline

Start
2023-02-27
Primary completion
2023-12-30
Completion
2024-03-30

Drugs

EvaluationDrugModalityDoseRoute
Comparator BRM421 Unknown — Topical

Indications