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This study revealed that treatment with FMD, administered three days prior to and during neoadjuvant chemotherapy, enhanced therapeutic efficacy without increasing toxicity or reducing chemotherapy-induced DNA damage in T cells

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Food and Drug Administration cleared Ascletis Pharma to start a Phase 1 clinical trial of ASC35 , a once-monthly subcutaneous peptide that activates both the GLP-1 and GIP receptors

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