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Subcutaneous and intraperitoneal routes have also been used in clinical protocols

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The authors themselves described it as a small preliminary study.[15] A 2025 pilot report described intravenous administration to two healthy adults at doses up to 20 mg, with no measurable changes in cardiac, hepatic, renal or thyroid biomarkers and no reported adverse effects.[16] Two individuals cannot characterise uncommon reactions, immunogenicity, long-term toxicity, reproductive safety or oncological risk

Differences in daily intake and supplemental forms can also influence their clinical use

It doesnt just protect cells