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

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Wyeth

Status and phase

Completed
Phase 2

Conditions

Postmenopausal Osteoporosis

Treatments

Drug: Placebo
Drug: Bazedoxifene

Study type

Interventional

Funder types

Industry

Identifiers

NCT00238745
3068A1-207

Details and patient eligibility

About

Dose-response in Japanese patients with postmenopausal osteoporosis.

Sex

Female

Ages

Under 85 years old

Volunteers

No Healthy Volunteers

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.

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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