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Description
The clinical doses represent systemic plasma concentrations achieved in humans following subcutaneous administration
As a result, the FDA concluded that these products were misbranded under sections 502(a) and 502(bb) of the FDCA [21 U.S.C
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[DOI] [PMC free article] [PubMed] [Google Scholar] 64.Imbernon M, Saponaro C, Helms HC, Duquenne M, Fernandois D, Deligia E, et al
2022, Garvey et al
