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. 2019 Jan 30;74(5):1348–1356. doi: 10.1093/jac/dky567

Table 4.

Simulated typical darunavir pharmacokinetic parameters and probability of therapeutic exposure for standard and doubled ritonavir boosting

AUCta (mg·h/L) AUCua (mg·h/L) C trough, t (mg/L) C trough, u (mg/L) Probability of TAt (%) Probability of TAu (%)
Pregnant (GA = 38 weeks)
 800/100 mg q24h 58 7.6 1.1 0.12 78 94
 600/100 mg q12h 82 11 2.1 0.25 96 99
 800/200 mg q24hb 59 7.7 1.1 0.12 80 94
 600/200 mg q12hb 83 11 2.1 0.28 96 100
 1200/100 mg q24hb 78 11 1.4 0.16 87 97
 800/100 mg q12hb 102 15 2.6 0.31 99 100
Non-pregnant
 800/100 mg q24h 76 8.0 1.6 0.14 92 97
 600/100 mg q12h 107 12 2.9 0.28 99 100
 800/200 mg q24hb 77 8.1 1.6 0.14 93 97
 600/200 mg q12hb 107 12 2.9 0.28 99 100
 1200/100 mg q24hb 102 12 2.1 0.19 96 98
 800/100 mg q12hb 132 16 3.5 0.35 100 100

GA, gestational age; Ctrough, concentrations at the end of the dosing interval; TA, therapeutic exposure; t, total; u, unbound.

a

Values refer to the daily exposure (0–24 h for both q24h and q12h dosing).

b

Explored darunavir/ritonavir dosing regimens.