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Clinical Trial Summary

This study will assess the antimyeloma effects of BHQ880A in patients with smoldering multiple myeloma with high risk of progression to active multiple myeloma. BHQ880 will be administered every 28 days in previously untreated patients. Disease assessments will be performed monthly and effects on bone metabolism will be assessed by measurement of serum and urine bone biomarkers, changes in BMD , and QCT with FEA. Additionally, the PK profile of BHQ880 as a single agent and following multiple doses will be obtained.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01302886
Study type Interventional
Source Novartis
Contact
Status Completed
Phase Phase 2
Start date May 2011
Completion date November 2013

See also
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