This prospective, Phase 3, open-label, study (EudraCT: 2016-001631-12) evaluated pharmacokinetic (PK) characteristics of 3-/4-weekly Privigen V R (IgPro10, CSL Behring, King of Prussia, PA, USA) in Japanese patients with PID. PK parameters including serum trough immunoglobulin (IgG) level before next infusion during the wash-in/wash-out phase (C trough), area under the concentration-time curve from time point zero to the last time point with quantifiable concentration (AUC 0-last), dose-adjusted AUC 0-last (dAUC), lowest and highest observed IgG levels (C min , C max), time to reach C max (T max), and total clearance (CL) were analyzed for both regimens of Privigen V R (dose: 138-554 mg/kg body weight). Ten patients were included in this analysis (3-/4-weekly: n ¼ 2/n ¼ 8). C trough levels achieved ranged 7.96-10.05 g/L. C max was observed approximately 1 h after the start of the infusion in both regimens. Mean (SD [not applicable for 3-weekly data]) PK parameters: C max , 16.60 and 14.20 (5.53) g/L; C min , 10.60 and 8.53 (3.89) g/L; AUC 0-last , 5971 and 6591 (2633) g à h/L; dAUC, 0.41 and 0.46 (0.19) g à h/L/ mg; CL, 2.53 and 2.53 (1.00) mL/h and median T max was 1.19 and 1.14 h, for 3-/4-weekly dosing regimens, respectively. Privigen V R PK characteristics in Japanese patients were similar between dosing regimens and to previously-reported results in non-Japanese patients with PID.