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Clinical Trial Summary

Clinical phase I, controlled, non comparative, open, single center study evaluating the safety and tolerability of ophthalmic solution PRO-172 when applied on the ocular surface of healthy volunteers.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04693429
Study type Interventional
Source Laboratorios Sophia S.A de C.V.
Contact
Status Completed
Phase Phase 1
Start date September 24, 2020
Completion date December 8, 2020

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