Table 2.
%fT>CT | fAUC0–24 (mg·h/L) | ||||||||
---|---|---|---|---|---|---|---|---|---|
Cefepime | |||||||||
CT (mg/L) | 4 | 8 | 16 | 32 | 64 | 128 | 256 | 512 | |
humana | 100 | 84 | 58 | 35 | 11 | 0 | 0 | 0 | |
mouse HSRb | 96 | 83 | 59 | 38 | 8 | 0 | 0 | 0 | |
Taniborbactam | |||||||||
CT (mg/L) | 0.25 | 0.5 | 1 | 2 | 4 | 8 | 16 | 32 | |
humanc | 100 | 100 | 100 | 100 | 80 | 51 | 17 | 0 | 229 |
moused 24:1 | 85 | 56 | 23 | 3 | 0 | 0 | 0 | 0 | 17.0 |
moused 12:1 | 99 | 85 | 56 | 23 | 3 | 0 | 0 | 0 | 33.9 |
moused 6:1 | 100 | 99 | 85 | 56 | 23 | 3 | 0 | 0 | 67.8 |
moused 4:1 | 100 | 100 | 88 | 64 | 33 | 8 | 0 | 0 | 101 |
moused 3:1 | 100 | 100 | 99 | 85 | 56 | 23 | 3 | 0 | 136 |
moused,e 2:1 | 100 | 100 | 100 | 100 | 84 | 53 | 16 | 0 | 204 |
Human exposures for a dose of 2 g q8h as a 2 h infusion estimated based on best-fit pharmacokinetic parameters of cefepime in healthy subjects from Phase I studies upon co-administration of taniborbactam.
Mouse exposure estimated based on best-fit pharmacokinetic parameters of cefepime in infected mice.
Human exposures for a dose of 0.5 g q8h as a 2 h infusion estimated based on best-fit pharmacokinetic parameters of taniborbactam in healthy subjects from Phase I studies.10
Mouse exposure estimated based on best-fit pharmacokinetic parameters of taniborbactam in infected mice. Ratios represent the proportions of cefepime:taniborbactam, relative to the doses of the cefepime HSR.
Mouse exposure was comparable to that achieved in humans and is denoted in bold.