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The trial used a 20-week bi-weekly dose escalation phase followed by a 26-week maintenance phase, for a total of 46 weeks

More clinical trials aimed at obese people in Asia and Africa are expected to prove its effectiveness and safety

It has the dual functions of "anti-oxidation" and "inhibition", to combat melanin in an all-around way

These restrictions may be more limiting for compounded products as compared with FDA-approved products regarding efficacy and safety claims.[21] Congress has granted FDA the authority to ensure that prescription drugs are safe and effective for the uses in the drugs labeling and has given FDA the explicit authority to oversee compounded drugs.[22] Under a 1971 Memorandum of Understanding with the FTC, FDA exercises primary responsibility for prescription drug advertising.[23] While compounded medications have different rules for labels, which are written, printed or graphic matter upon the immediate container of a drug[24], compounded drugs are subject to the same FDCA requirements as prescription drugs for labeling, advertising, and promotion.[25] Finally, the APC has asserted that labeling applies to the physical drug container and ancillary written materials (like package inserts)

2017;6:e29985

PMID 19136143