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July 20: Four years after it was rejected by the FDA due to safety concerns, Daiichi Sankyos Vanflyta (quizartinib) won approval to treat patients with acute myeloid leukemia that has a FLT3-ITD gene mutation

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The FDA has restricted compounding pharmacies from producing BPC-157 due to safety concerns, and the World Anti-Doping Agency classifies it as an S0 Unapproved Substance. Manufacturing and distribution are largely underground, raising quality control concerns for black-market products

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