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The difference was 17.9% (95% CI -2 to 37.7; P=.08). Subjects (n=69) at the 21 US sites not participating in the AI substudy had cumulative pharmacokinetic adherence over 24 weeks of 78.1% (SD 29.7). The analysis set consisted of all subjects who received any dose of ABT-126 at US sites selected to use the AI Platform and who had available pharmacokinetic data. Visits were based on a categorization of collection day data into weekly windows.
Earle E Ellen Bain, Laura Shafner, David P Walling, Ahmed A Othman, Christy Chuang-Stein, John Hinkle, Adam Hanina
JMIR Mhealth Uhealth 2017;5(2):e18Download Citation: END BibTex RIS