Overview Dose Response Study of Lasofoxifene in Postmenopausal Women With Osteoporosis - Japanese Asian Dose Evaluation Status: Completed Trial end date: 2006-03-01 Target enrollment: Participant gender: Summary To establish the optimal dose of lasofoxifene that is fully effective in increasing the BMD in postmenopausal Asian women. Phase: Phase 2 Details Lead Sponsor: Ligand Pharmaceuticals