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The fourth component, GHK-Cu, will be voted on in a subsequent February 2027 meeting HHS has announced that GHK-Cu is expected to return to Category 1 (after being moved to Category 2 in September 2023), which would restore compounding access for injectable formulations. The recommendations of the PCAC are non-binding but noteworthy

The package contains a lot-specific Certificate of Analysis covering HPLC purity, LC-MS identity, disulfide bond integrity, and the LAL endotoxin reading, along with a Safety Data Sheet and a brief handling reference

Schedule: Weekly subcutaneous injections for 1248 weeks (clinical trials ranged 3648 weeks) [2]