Clinical Trial SuccessThe ENLIGHTEN 2 study met its primary and key secondary endpoints, renewing hope for LYR-210.
Market OpportunityIf the pursuit of LYR-210 FDA approval focuses on the CRSsNP patient population, it targets roughly 70% of CRS patients, which represents a significant portion of the market.
Regulatory SimplificationFDA agreed to the use of a single primary endpoint of change from baseline in the 3 cardinal symptoms score, which simplifies the study requirements.