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People are injecting substances from suppliers they found on Google into their bodies with no independent verification of what's actually in the vial

D., Burgess, D., & Gamzu, E

Food and Drug Administration) Separately, FDA documentation around the 503A bulks process shows AOD-9604s status has moved around as nominations were withdrawn and advisory committee discussions occurred

Ive personally used both protocols extensively and tracked the outcomes in thousands of individuals

Patients will be randomised (1:1) by minimisation on age, mRS, NIHSS, type of centre and time from onset, to receive 10mg of MCL/placebo (normal saline 2ml) tds via injection or nasogastric tube for 14 days