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The commentators point out that the research may not be fully accounting for a persistent imbalance in HbA1c levels in subjects and BMI may tend toward bias in prescribing patterns for these drugs, despite using propensity score matching

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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

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