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The primary safety endpoints are the proportion of patients with any treatment-emergent adverse events (TEAEs) related to study RBC transfusion through 28 days, and the proportion of patients with treatment-emergent antibodies with confirmed specificity to pathogen-reduced RBCs through 75 days after the last study transfusion
Peptide Content: 15mg Bepecin Arginate Salt, 15mg TB-500 (Ac-SDKP), 30mg GHK-CU per bottle
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