Status:
COMPLETED
A Study to Evaluate the Safety, Tolerability, and Efficacy of an Investigational Drug and Dietary Supplement in Men and Postmenopausal Women With Osteoporosis (0217A-227)
Lead Sponsor:
Organon and Co
Conditions:
Osteoporosis
Vitamin D Deficiency
Eligibility:
All Genders
40-90 years
Phase:
PHASE3
Brief Summary
The purpose of this study is to test the safety, tolerability and effectiveness of an investigational drug and dietary supplement to reduce the risk of vitamin D insufficiency and deficiency during th...
Eligibility Criteria
Inclusion
- Men or postmenopausal women who are osteoporotic
Exclusion
- Vitamin D deficiency
- Other disease of bone or mineral metabolism
- Digestive disease causing malabsorption
- Other significant medical conditions that are not adequately treated
Key Trial Info
Start Date :
September 24 2003
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
May 1 2004
Estimated Enrollment :
717 Patients enrolled
Trial Details
Trial ID
NCT00092066
Start Date
September 24 2003
End Date
May 1 2004
Last Update
August 14 2024
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