Where FDA has identified limitations in its authority, the industry must lead with safety and transparencythrough verified sourcing, meaningful identity and potency testing, defined impurity standards, traceability, responsible clinical protocols, adverse-event reporting, and honest communication about what is known and what remains uncertain
TB-500 is usually a fragment, not the studied protein
Khorram, O., Laughlin, G
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Immunological effects of thalidomide and its chemical and functional analogs
