Figure 2.
Coprimary endpoints. (A) Primary lymphadenopathy endpoint: least square mean of the change from baseline at D85 in the log10-transformed sum of product diameters of the index lymph node lesions in the PD analysis set (leniolisib, n = 18; placebo, n = 8). One patient in the leniolisib group was excluded because of complete resolution of lesions by D85 (0 mm), therefore the log10 transformation could not be computed. Compared with placebo, leniolisib reduced lymphadenopathy (P = .0006). (B) Primary naïve B-cell endpoint: least square mean of the change from baseline at D85 in the percentage of naïve B cells (CD19+CD27-CD10-) out of total B CD19+ cells in the B-PD analysis set (leniolisib, n = 8; placebo, n = 5). Compared with placebo, leniolisib increased naïve B-cell levels (P = .0002). Error bars are SEM. ∗∗∗P ≤ .001. CFB, change from baseline; SEM, standard error of mean.

Coprimary endpoints. (A) Primary lymphadenopathy endpoint: least square mean of the change from baseline at D85 in the log10-transformed sum of product diameters of the index lymph node lesions in the PD analysis set (leniolisib, n = 18; placebo, n = 8). One patient in the leniolisib group was excluded because of complete resolution of lesions by D85 (0 mm), therefore the log10 transformation could not be computed. Compared with placebo, leniolisib reduced lymphadenopathy (P = .0006). (B) Primary naïve B-cell endpoint: least square mean of the change from baseline at D85 in the percentage of naïve B cells (CD19+CD27-CD10-) out of total B CD19+ cells in the B-PD analysis set (leniolisib, n = 8; placebo, n = 5). Compared with placebo, leniolisib increased naïve B-cell levels (P = .0002). Error bars are SEM. ∗∗∗P ≤ .001. CFB, change from baseline; SEM, standard error of mean.

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