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Sponsored by: |
Eli Lilly and Company |
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Information provided by: | Eli Lilly and Company |
ClinicalTrials.gov Identifier: | NCT00085956 |
The purposes of this study are to determine:
Condition | Intervention | Phase |
---|---|---|
Postmenopausal Bone Loss |
Drug: Arzoxifene Drug: Placebo |
Phase III |
Study Type: | Interventional |
Study Design: | Prevention, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study |
Official Title: | Effects of Arzoxifene on Bone Mineral Density and Endometrial Histology in Postmenopausal Women. |
Estimated Enrollment: | 300 |
Study Start Date: | April 2004 |
Estimated Study Completion Date: | February 2007 |
Ages Eligible for Study: | 45 Years to 60 Years |
Genders Eligible for Study: | Female |
Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
Exclusion Criteria:
United States, California | |
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559), Mon - Fri 9 AM to 5 PM Eastern time (UTC/GMT - 5 hours, EST), or speak with your personal physician. | |
San Diego, California, United States, 92103 |
Study Director: | Call 1-877-CTLILLY(1-877-285-4559) or 1-317-615-4559 Mon - Fri 9 AM - 5 PM Eastern time (UTC/GMT - 5 hours, EST) | Eli Lilly and Company |
Study ID Numbers: | 8537, H4Z-MC-GJAE |
Study First Received: | June 18, 2004 |
Last Updated: | March 7, 2007 |
ClinicalTrials.gov Identifier: | NCT00085956 |
Health Authority: | United States: Food and Drug Administration |
Musculoskeletal Diseases Osteoporosis, Postmenopausal Osteoporosis Bone Diseases, Metabolic Bone Diseases |