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Safety Study of an Oral Pro-boneTM, Administered to Post Menopausal Osteopenic Women

Osteopenia Clinical Trial

Official title:
Phase 1 Study of an Oral Pro-boneTM, Administered to Post Menopausal Osteopenic Women

Clinical Trial Summary

Recent studies have shown that inhibition of Aquaporine-9 channels may ameliorate the bone degradation process. Pro-bone is an AQ - 9 channels inhibitor. This study is design to evaluate the safety of Pro-bone.

Clinical Trial Description

n/a

Study Design

Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01397838
Study type Interventional
Source OsteoBuild Ltd.
Contact
Status Not yet recruiting
Phase Phase 1
Start date September 2011
Completion date January 2012
View Details
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