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Gimbrone MA Jr, Topper JN, Nagel T, Anderson KR, Garcia-Cardena G

"We emphasize that as the clinical investigator, it is your responsibility to ensure that studies are conducted in accordance with the investigational plan, both to protect the rights, safety, and welfare of subjects and to ensure the integrity of study data." FDA noted that two of the nine randomized subjects who received the investigational product were not eligible under the enrollment criteria

doi: 10.1007/s00285-022-01835-y 52

Biochimica et

As awareness grows, informal human trials are expected to increase, especially within the longevity community (eLife)(HowStuffWorks)
10.1161/01.ATV.0000105902.89459.09
