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Efficacy and Safety of LYR-210 for the Treatment of Chronic Rhinosinusitis in Adults (ENLIGHTEN 2)

← catalyst calendar

NCT05295459 · results posted

Sponsored by Lyra Therapeutics (industry) · LYRA — their whole pipeline →.

Phase
Phase 3
Status
Completed
Study type
Interventional
Design
Randomized · Double · Treatment
Enrollment
182actual
Sites
57
Countries
Belgium, Bulgaria, Germany +3

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2022-05-13actualWhen the study began enrolling
Primary completion2025-04-02actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2025-04-02actualThe whole study's end, after follow-up
First posted2022-03-25actualWhen this record first appeared on the registry
Results posted2026-02-19actualWhen the sponsor posted results to the registry
Record updated2026-02-19actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Chronic Sinusitis
  • Chronic Rhinosinusitis (Diagnosis)

Interventions

  • Drug: LYR-210
  • Drug: Sham procedure control
  • Other: Background therapy

Primary outcome

what the primary-completion date above is the date OF
Change From Baseline (CFBL) in the 7-day Average Composite Score of 3 Cardinal Symptoms (3CS) in Participants Without Nasal Polyps
measured Week 24

Posted documents

hosted by the registry — we link, never re-serve
Study Protocolposted 2024-03-29 · 1.5 MB · Prot_002.pdf
Statistical Analysis Planposted 2025-02-06 · 748 KB · SAP_003.pdf

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