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Dihexa has not been tested in large-scale human clinical trials and does not hold FDA approval for any indication

Doses exceeding ~200300 mg/day should generally be reserved for supervised therapeutic use due to potential for metabolic byproduct accumulation [15]

In the future, there is a need to combine multi-omics technology to analyze the metabolic heterogeneity, develop multiple inhibitors targeting the compensatory pathway, and improve the killing effect of cancer cells through the combination of glutamine metabolism inhibition with immune checkpoint blockade, CAR-T therapy, and other applications

Sci Rep (2018) 8:4564

You might be transitioning from semaglutide to tirzepatide