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Clinical Trial Summary

Volunteer participants are evaluated for eligibility during a Screening Visit; those meeting study inclusion/exclusion criteria are scheduled for 2 treatment visits. At each treatment visit, 1 of the 2 study treatments is self-administered to both eyes. Afterwards, efficacy and safety assessments are performed over a 3-hour period.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05114486
Study type Interventional
Source Eyenovia Inc.
Contact Greg Bennett, MSEd
Phone 650-504-2005
Email [email protected]
Status Recruiting
Phase Phase 3
Start date November 3, 2021
Completion date April 30, 2022

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