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Clinical Trial Summary

After screening, eligible subjects will be scheduled for 2 treatment visits where either 1 mist or 2 mists of the study drug will be administered to both eyes according to a pre-specified randomization plan. Safety evaluations and efficacy measurements will be performed at specified time intervals thereafter. Pupil dilation for each treatment will be compared at each time interval.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04907474
Study type Interventional
Source Eyenovia Inc.
Contact
Status Completed
Phase Phase 4
Start date May 24, 2021
Completion date June 3, 2021

See also
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