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Storage delays

Future studies will need to examine in more detail also the impact of specific CaP stages and treatments on the contribution of ncRNAs to AR action

Accessed April 24, 2024.

No validated human protocols exist

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In the double-blind, randomized, placebo-controlled, dose-escalation phase 1 study of ASHMI (600 mg, 1200 mg, 1800 mg), no grade 3 adverse events occurred, laboratory parameters before and after treatment remained within normal ranges, and no unexpected immunological changes were detected, supporting its safety and tolerability allowing for advancement to phase 2 study [99]