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VBI-2901 is being examined in Phase-I trials

An interesting avenue of research comes from work in the carcinoid syndrome

Stable shRNA lentiviral transfection c-Met shRNA (sh c-Met), mTOR shRNA (sh mTOR), and negative control shRNA (sh NC) were cloned into GV248 lentiviral vectors, which are powerful tools for modifying the genes of eukaryotic cells

The solution will be blue to blue-violet, from the d-d transition of the Cu(II) centre, and this is expected

And for the broader project of longevity medicine building a clinical practice that optimizes biology rather than reacting to disease the return of these compounds to legitimate access is a step in the right direction