Table 6. Pharmacokinetics of DB829 Pharmacokinetics of DB829 in vervet monkeys with second stage HAT after the 10th oral dose of DB868.
Monkey | Tmax (day) | Cmax (nmol/L) | AUC0–63 (nmol/L•day) | t½ (day) | |
---|---|---|---|---|---|
20 mg/kg × 10 days | 573F | 1 | 460 | 7700 | 48 |
679F | 0.33 | 630 | 13000 | NC ‡ | |
689M | 0.17 | 500 | 4700 | 180 | |
696M | 0.17 | 530 | 5900 | NC ‡ | |
10 mg/kg × 10 days | 688M | 0.04 | 410 | 2500 | NC ‡ |
690F | 2.0 | 340 | 5100 | 120 | |
695M | NC* | NC* | NC* | NC* | |
697F | 0.33 | 210 | NC † | NC † | |
3 mg/kg × 10 days | 670F | 0.33 | 60 | NC † | NC † |
687M | 0.33 | 110 | 1800 | NC ‡ |
Tmax, time to reach Cmax; Cmax, maximum concentration; AUC0–63, AUC from 0 to 63 days; t½, terminal half-life; F, female; M, male; NC, not calculable;
* = data was too sparse to determine the Tmax, Cmax, AUC0–63, and t½ with confidence;
† = data was too sparse to determine the AUC0–63, and t½ with confidence;
‡ = data was insufficient in the terminal phase to determine the t½ with confidence.