Table 5.
Age strata, years | All patients | Post‐menopausal BMD in the absence of elagolix treatment | ||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
<25th percentile | 25th to 75th percentile | >75th percentile | ||||||||||
Not treated with elagolix | Treated with elagolix | Difference | Not treated with elagolix | Treated with elagolix | Difference | Not treated with elagolix | Treated with elagolix | Difference | Not treated with elagolix | Treated with elagolix | Difference | |
150 mg QD for 12 months | ||||||||||||
Patients who met criteria for antiosteoporosis treatment, N (%) | ||||||||||||
50–59 | 21 (2.53%) | 24 (2.89%) | 3 (0.36%) | 17 (8.29%) | 20 (9.76%) | 3 (1.46%) | 4 (0.96%) | 4 (0.96%) | 0 (0.00%) | 0 (0.00%) | 0 (0.00%) | 0 (0.00%) |
60–69 | 70 (8.14%) | 72 (8.37%) | 2 (0.23%) | 56 (26.17%) | 58 (27.1%) | 2 (0.93%) | 14 (3.24%) | 14 (3.24%) | 0 (0.00%) | 0 (0.00%) | 0 (0.00%) | 0 (0.00%) |
70–79 | 241 (39.31%) | 252 (41.11%) | 11 (1.79%) | 139 (90.85%) | 143 (93.46%) | 4 (2.61%) | 97 (31.6%) | 103 (33.55%) | 6 (1.95%) | 5 (3.27%) | 6 (3.92%) | 1 (0.65%) |
200 mg QD for 3 months | ||||||||||||
Patients who met criteria for antiosteoporosis treatment, N (%) | ||||||||||||
50–59 | 21 (2.53%) | 24 (2.89%) | 3 (0.36%) | 17 (8.29%) | 20 (9.76%) | 3 (1.46%) | 4 (0.96%) | 4 (0.96%) | 0 (0.00%) | 0 (0.00%) | 0 (0.00%) | 0 (0.00%) |
60–69 | 70 (8.14%) | 72 (8.37%) | 2 (0.23%) | 56 (26.17%) | 58 (27.1%) | 2 (0.93%) | 14 (3.24%) | 14 (3.24%) | 0 (0.00%) | 0 (0.00%) | 0 (0.00%) | 0 (0.00%) |
70–79 | 241 (39.31%) | 251 (40.95%) | 10 (1.63%) | 139 (90.85%) | 143 (93.46%) | 4 (2.61%) | 97 (31.6%) | 103 (33.55%) | 6 (1.95%) | 5 (3.27%) | 5 (3.27%) | 0 (0.00%) |
Patients met the threshold to initiate antiosteoporosis treatment if their 10‐year predicted risk of hip fracture was ≥3% or 10‐year probability of major osteoporotic fracture was ≥20%.
BID = Twice daily; QD = once daily.