Fig. 4From: An open-label phase 2 trial to assess the efficacy, safety and pharmacokinetics of lanthanum carbonate in hyperphosphatemic children and adolescents with chronic kidney disease undergoing dialysisLC plasma concentrations for patients after a single oral dose (part 1, n = 20). Pharmacokinetic set 1 included all patients from safety analysis set 1 who had at least one measurable plasma concentration of LC post-dose. Patients with LC plasma concentrations below the lower limit of quantification (0.05 ng/mL) were not included at the respective time points; lower SD error bars have been omitted for clarityLC lanthanum carbonate, SD standard deviationBack to article page