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Just 1 treatment every 710 days

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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

This inherent limitation underscores the urgent need for more effective therapeutic strategies

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NADPH is required for and consumed during fatty ...