Table 3.

Summary of plasma PK parameters of PEV in combination with IV/SC AZA: dose escalation

20-mg/m2 IV cohort (n = 6)30-mg/m2 SC cohort (n = 3)
Cycle 1, day 1   
 Tmax, h 1.06 (0.97-2.27) 0.98 (0.97-1.00) 
 Cmax, ng/mL 158 (51.4) 299 (29.9) 
 AUC24, ng/h per mL 990 (28.0) 1640 (26.4) 
 AUC48, ng/h per mL 1110 (30.6) 1770 (25.8) 
 t1/2, h 7.80 (1.13) 7.39 (0.699) 
Cycle 1, day 5   
 Tmax, h 0.99 (0.97-1.48) * 
 Cmax, ng/mL 165 (48.4) — 
 AUC24, ng/h per mL 986 (38.4) — 
 AUC48, ng/h per mL 1090 (35.6) — 
 t1/2, h 7.98 (0.818) — 
20-mg/m2 IV cohort (n = 6)30-mg/m2 SC cohort (n = 3)
Cycle 1, day 1   
 Tmax, h 1.06 (0.97-2.27) 0.98 (0.97-1.00) 
 Cmax, ng/mL 158 (51.4) 299 (29.9) 
 AUC24, ng/h per mL 990 (28.0) 1640 (26.4) 
 AUC48, ng/h per mL 1110 (30.6) 1770 (25.8) 
 t1/2, h 7.80 (1.13) 7.39 (0.699) 
Cycle 1, day 5   
 Tmax, h 0.99 (0.97-1.48) * 
 Cmax, ng/mL 165 (48.4) — 
 AUC24, ng/h per mL 986 (38.4) — 
 AUC48, ng/h per mL 1090 (35.6) — 
 t1/2, h 7.98 (0.818) — 

All patients on the dose-escalation cohorts received IV PEV (20 mg/m2 cohort, n = 6; 30 mg/m2 cohort, n = 3). Parameters are presented as geometric mean (% coefficient of variation) unless specified otherwise; Tmax (median and range); t1/2 (mean and standard deviation).

*

Not reported; only 1 patient was evaluable on cycle 1, day 5, as dosing was halted due to AEs.

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