Proof of Concept (Bone Resorption/Bone Mineral Density) Study (0429-005)

Phase 2

Completed

• Conditions: Post-Menopausal Osteoporosis

• Registration Number: NCT00533650
• Lead Sponsor: Merck Sharp & Dohme LLC

Brief Summary

A study to asses the safety and efficacy of MK0429 in postmenopausal women with osteoporosis.

Detailed Description

Not available

Basic Information
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Recruitment & Eligibility
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Study & Design

Study Timeline

• Study Start: 2000-12
• Primary Completion: 2002-10
• Study Completion: 2002-10
• Study First Submitted: 2007-09-19
• Study First Submitted QC: 2007-09-19
• Study First Posted: 2007-09-21
• Status Verified: 2016-05
• Last Update Submitted: 2016-07-28
• Last Update Posted: 2016-07-29

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 227

Inclusion Criteria

• Person is a women with osteoporosis who is unwilling or unable to take other treatments for osteoporosis

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Exclusion Criteria

• Person has had a previous fracture
• Person has rheumatoid arthritis. Person has has certain types of cancer
• Person has donated blood or has been in another investigational study within the last 4 weeks

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL