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Zero human trials

The Consolidated Appropriations Act, 2021, Public Law 116-260, division CC, section 401(c), amended section 1847A(f)(A) to state that, manufacturers of drug or biological including items, services, supplies, and products that are payable under Medicare Part B as a drug or biological that have not entered into a National Medicaid Drug Rebate Agreement are required to report ASP (and WAC) data to CMS

It happens after GLP-1 fat loss treatment , after bariatric surgery, after crash diets, after severe caloric restriction of any kind

Its website states that compounded versions are not FDA-approved, which is a disclosure many clinics either bury or omit entirely