Study Comparing Arzoxifene With Raloxifene in Women After Menopause With Osteoporosis
NCT ID: NCT00383422
Last Updated: 2010-01-28
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE3
320 participants
INTERVENTIONAL
2006-10-31
2008-07-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
QUADRUPLE
Study Groups
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1
Arzoxifene
20 mg, oral, tablet, once a day for 52 weeks
2
Raloxifene
60 mg, oral, tablet, once a day for 52 weeks
Interventions
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Arzoxifene
20 mg, oral, tablet, once a day for 52 weeks
Raloxifene
60 mg, oral, tablet, once a day for 52 weeks
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Must be between 50 and 75 years old and be able to walk
* Have at least two of your back bones that can be x-rayed
* Have not had a period in at least two years
* Be willing to have blood tests
Exclusion Criteria
* History of estrogen dependent cancer
* History of stroke or certain heart problems
* Possibly have an allergy to raloxifene or arzoxifene
* Have certain abnormal lab values
* History of seizure disorder
* Have unexplained vaginal bleeding or an abnormal pap smear
50 Years
75 Years
FEMALE
No
Sponsors
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Eli Lilly and Company
INDUSTRY
Responsible Party
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Eli Lilly
Principal Investigators
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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)
Role: STUDY_DIRECTOR
Eli Lilly and Company
Locations
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For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Gainesville, Georgia, United States
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Urbandale, Iowa, United States
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Billings, Montana, United States
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Cincinnati, Ohio, United States
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Houston, Texas, United States
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Buenos Aires, , Argentina
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Randwick, New South Wales, Australia
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Vancouver, British Columbia, Canada
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Halifax, Nova Scotia, Canada
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Toronto, Ontario, Canada
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Québec, Quebec, Canada
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Amiens, , France
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Orléans, , France
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Vandœuvre-lès-Nancy, , France
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Rome, , Italy
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Torino, , Italy
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Barcelona, , Spain
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Madrid, , Spain
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Changhua, , Taiwan
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Taipei, , Taiwan
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Taoyuan District, , Taiwan
Countries
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Other Identifiers
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H4Z-MC-GJAR
Identifier Type: OTHER
Identifier Source: secondary_id
8580
Identifier Type: -
Identifier Source: org_study_id
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