78) −2.14 (0.77) −1.55 (0.96) Total hip BMD T-score −1.44 (0.71) −1.42 (0.69) −1.21 (0.73) One-third BMD T-score −1.48 (1.21) −1.48 (1.18) −1.35 (1.19) Albumin-adjusted calcium, mg/dL 9.77 (0.37) 9.77 (0.37) 9.86 (0.37) Creatinine, mg/dL 0.76 (0.15) 0.76 (0.15) 0.83 (0.16) Subjects who completed, n (%) 262 (64 %) 203 (64 %) 138 (69 %) Values are mean (SD) unless indicated otherwise BMD and BTM assessments Continued denosumab treatment cohort For the subjects who received 8 years of continued denosumab treatment and had evaluable

data, BMD at the lumbar spine and total hip significantly increased during the 4 years of the see more extension study, while the BMD at the one-third radius remained stable (Fig. 2). Compared with the parent study baseline, eight continued years of denosumab treatment was associated with mean BMD changes of 16.5, 6.8, and 1.3 % at the lumbar spine,

total hip, and one-third radius, respectively (Fig. 2), Quisinostat purchase and 6.8 % at the femoral neck (data not shown). From the extension study baseline, BMD increased at the lumbar spine by 5.7 % (Fig. 2a), total hip by 1.8 % (Fig. 2b), one-third radius by 0.8 % (Fig. 2c), and femoral neck by 2.3 % on average (data not shown). At the end of year 8, the serum CTX and BSAP remained below parent study baseline with median reductions of 65 and 44 %, respectively (Fig. 3). The levels of reduction in both CTX and BSAP at the end of the dose interval were similar at all time points in the study extension. Fig. 2 Effect of 8 years of continued denosumab treatment AG-881 mouse on BMD at the a lumbar spine, b total hip, and c one-third radius. BMD values are shown as percent change from parent study baseline (LSM + 95 % CI based on ANCOVA models adjusting IKBKE for geographical location and parent study baseline BMD values). Gray boxes indicate the

original 4-year parent study. Numbers shown at each time point reflect the number of subjects enrolled in the extension study with observed data at the selected time points of interest Fig. 3 Effect of 8 years of continued denosumab treatment on levels of a serum CTX and b BSAP. Bone turnover markers are shown as actual values (medians with Q1 to Q3 interquartile ranges). Gray boxes indicate the original 4-year parent study. Numbers shown at each time point reflect the number of subjects enrolled in the extension study with observed data at the selected time points of interest. Asterisk A calibration discrepancy at the central laboratory may have led to BSAP results in some individual samples to be falsely elevated by up to 14 % at months 90 and 96 Previous placebo cohort In the subjects who received placebo during the 4-year parent study, BMD increased at the lumbar spine, total hip, and femoral neck with 4 years of denosumab treatment in the extension study. From the extension study baseline, BMD increased by 11.9 % at the lumbar spine (Fig. 2a), 5.6 % at the total hip (Fig. 2b), and 4.0 % at the femoral neck on average (data not shown).