Figure 6(a) shows that the combined results of two separate experiments (n = 10 mice/treatment) recapitulate the data seen in Figure 5(b) , indicating that the protection afforded by FP12 is highly significant when administered by either the i.v. or i.p. routes.
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Preclinical development of the TLR4 antagonist FP12 as a drug lead targeting the HMGB1/MD-2/TLR4 axis in lethal influenza infection.
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