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