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Clinical Trial Summary

Multicenter, phase III, randomized, blinded, controlled, parallel group.


Clinical Trial Description

This is a 24-week, multicenter, phase III, randomized, blinded, controlled, parallel group with a 24-week treatment period to evaluate the efficacy and safety of LYR-210 compared with sham control for treatment in adults with CRS. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05295459
Study type Interventional
Source Lyra Therapeutics
Contact Lyra Clinical
Phone 617-393-4600
Email lyraclinical@lyratx.com
Status Recruiting
Phase Phase 3
Start date May 13, 2022
Completion date December 15, 2024

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