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. 2014 Mar 13;2(2):e00033. doi: 10.1002/prp2.33

Table 1.

Baseline characteristics (safety population).

Characteristic Group A (midazolam + denosumab*) (N = 19) Group B (Midazolam Alone) (N = 8)
Gender, n (%)
 Female 19 (100.0) 8 (100.0)
Race, n (%)
 White 17 (89.5) 6 (75.0)
 Black/African American 1 (5.3) 1 (12.5)
 Asian 1 (5.3) 1 (12.5)
Age (years)
 Mean (SD) 64.4 (6.16) 66.3 (5.34)
 Range 55–73 59–75
 ≥65 years, n (%) 12 (63.2) 4 (50.0)
Bone mineral density T-score, mean (SD)
 Total hip −2.07 (0.68) −2.15 (0.65)
 Lumbar spine −2.96 (0.76) −2.68 (0.92)

SD, standard deviation.

*

Midazolam 2 mg orally on day 1 and day 16, and denosumab 60 mg subcutaneously on day 2.

Midazolam 2 mg orally on day 1 and day 16.