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. 2022 Jan 1;42(3):500–511. doi: 10.1007/s10875-021-01181-6

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© The Author(s) 2021, corrected publication 2022

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Fig. 1 — Subject Disposition^a. ^aOne subject who was screened and entered into the previous regimen phase was withdrawn at sponsor’s request prior to receiving any amount of IGSC 20% due to reported serious adverse events (non-productive cough with accompanying cyanosis, hypoxemia, interstitial pneumonitis) ^bRefers to the first 13 weeks of treatment ^cRefers to the next 39 weeks of treatment