drugset / Trial / NCT05393895

An Evaluation of the Safety of CSF-1 in Presbyopic Subjects

NCT05393895 ↗

Phase 3 Completed 178 enrolled Orasis Pharmaceuticals Ltd.
RandomizedParallel-groupDouble-blindTreatment

Summary

This is a multi-center, double-masked, vehicle-controlled study. The purpose of the study is to evaluate the safety of CSF-1 compared with vehicle in presbyopic subjects. Subjects will be treated for at least 6 weeks.

Timeline

Start
2022-04-22
Primary completion
2022-12-01
Completion
2022-12-01

Drugs

EvaluationDrugModalityDoseRoute
Subject CSF-1 Unknown — Other

Indications