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Unlike traditional blood glucose monitoring methods, CGMS offers continuous monitoring over a 24-hour period

This was Citius second try for FDA approval, after the regulator rejected Lymphir in July 2023, outlining the need for enhanced product resting requirements. In its resubmitted data package, the company included findings from the from the Phase III Study 302 trial, where treatment with the drug led to an objective response rate of 36.2%, with 8.7% reaching complete response

Disclaimer This blog post is for informational purposes only and should not be considered medical advice

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It is not a therapeutic drug and remains a research compound in 2026