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Ma et al., 2006

Wysham CH, Lin J, Kuritzky L

4 More recently, the FDA Reauthorization Act of 2017 (FDARA) made a reference encouraging the enrollment of more diverse patient populations, and the Final Rule for Clinical Trials Registration and Results Information Submission (42 CFR Part 11) went into effect in January 2017

These compounds are not intended for human consumption, medical use, or diagnostic purposes

Melanotan I is still treated as a research chemical and we thus cannot draw conclusions about its safety

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