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The modified Rankin Scale (mRS) at 90 days was missing for 3 (4.3%) patients in the semaglutide group and 2 (2.8%) patients in the standard therapy group due to loss to follow-up (Table S2)

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FDA Has Flagged CJC-1295 Safety Concerns The FDA has identified serious adverse events associated with CJC-1295, including increased heart rate and systemic vasodilatory reaction, and has highlighted concerns about immunogenicity, peptide-related impurities, and limited clinical data

HR: 0.66, 95% CI: 0.421.03)

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An atlas is available to facilitate the visual diagnosis of Hunner lesions, since variations in cystoscopic appearance have been reported