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Because of its potency, IV glutathione must always be administered under medical supervision, following proper assessment, dosing protocols, and safety standards

AOD-9604 FDA Approval History At a glance FDA approval status / Never approved for any indication in the United States NDA filing history / No New Drug Application has ever been submitted to FDA Chemical identity / Synthetic peptide corresponding to amino acids 176-191 of human growth hormone, with a tyrosine residue added at the C-terminus Developer / Metabolic Pharmaceuticals Ltd (Melbourne, Australia), now defunct Clinical trial outcome / Phase IIb trial (2007) failed to meet primary efficacy endpoint for obesity FDA compounding status / Placed on Category 2 list

Each of these functions has been shown in many contexts to be relevant for cancer pathogenesis

Mater Today Proc 3(6):19491957 Sarkar B, Verma SK, Akhtar J, Netam SP, Gupta SK, Panda PK, Mukherjee K (2018) Molecular aspect of silver nanoparticles regulated embryonic development in Zebrafish (Danio rerio) by Oct-4 expression