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Clinical Trial Summary

The primary objective of this study is to provide safety data for two different dosages of HydroLenz. Secondary objectives are to provide preliminary data to determine whether HydroLenz has the same effect in humans as it does in the porcine model; to confirm the reliability of methods for evaluating lens opacity; and, to acquire information that can be used to design the pivotal study.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05592912
Study type Interventional
Source PromiSight, LLC
Contact Jodi S Pitcher
Phone 513-961-8200
Email jlpitcher@crc-regulatory.com
Status Not yet recruiting
Phase Phase 1
Start date January 1, 2024
Completion date January 1, 2025

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