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For injectable GHK-Cu, dosing should only be set by a qualified healthcare provider

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

That's why she says it's important for people to closely monitor their social media use, including their intended time spent versus reality, as well as how they feel before, during, and after scrolling

No long-term contracts

A summary of the study characteristics and study quality can be found in Table 1 and Supplementary Material 3 respectively