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Clinical Trial Summary

This study will examine the efficacy and safety of tivanisiran sodium eye drops versus vehicle after a 2-week run-in phase when dosed once daily for 3 months in subjects with signs and symptoms of dry eye disease (DED) due to Sjögren's Syndrome.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04819269
Study type Interventional
Source Sylentis, S.A.
Contact
Status Completed
Phase Phase 3
Start date May 25, 2021
Completion date December 11, 2023

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