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Early-stage research suggests intranasal dihexa may achieve therapeutic CNS concentrations with minimal systemic exposure, potentially extending the effective half life at the target site (hippocampus) while reducing plasma half life

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This applies to glucose-metabolizing enzymes (e.g., hexokinase, aldolase, lactate dehydrogenase, phosphofructokinase, and PDH), which increase considerably in activity between the ages of 15 and 30 days (Takagaki, 1974

390 Other clinical studies focusing on providing additional drug options for HR+ advanced breast cancer patients following CDK4/6 inhibitor use are currently ongoing within the realm of PI3K/AKT/mTOR pathway inhibitors