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Anecdotal reports frequently describe dramatic early responses, with multiple users noting they thought improvements were placebo on day two but by day three the changes became undeniable

7A and Supplementary Figure S4)

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they found that the c-MET inhibitor tivantinib reduces the synthesis of GSK3 by inhibiting MET activation, thereby stabilizing the expression of PD-L1 and blocking T cell-mediated cytotoxicity [139]

But even with half-unit syringes, reconstitution volume matters: a 2mg dose from a 50mg/mL concentration requires 0.04mL (4 units)