Overview

Study Evaluating Bazedoxifene Dose-Response in Japanese Patients With Postmenopausal Osteoporosis.

Status:
Completed
Trial end date:
2007-03-01
Target enrollment:
0
Participant gender:
Female
Summary
Dose-response in Japanese patients with postmenopausal osteoporosis.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Wyeth is now a wholly owned subsidiary of Pfizer
Treatments:
Bazedoxifene
Criteria
Inclusion Criteria:

- Must be postmenopausal and diagnosed as osteoporosis based on bone mineral density
and/or vertebral fracture.

Exclusion Criteria:

- Diseases which possibly induce secondary osteoporosis or osteopenia and affect on bone
metabolism.