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Clinical trial

An Open-Label, Multi-Center Study to Determine Level of Adherence to Monthly Oral or Every Three Month Intravenous Ibandronate Treatment in Post-Menopausal Women With Osteoporosis or Osteopenia, Who Are GI Intolerant of Daily or Weekly Alendronate or Risendronate

NCT02598453 is registered in ClinicalTrials.gov with Hoffmann-La Roche as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
An Open-Label, Multi-Center Study to Determine Level of Adherence to Monthly Oral or Every Three Month Intravenous Ibandronate Treatment in Post-Menopausal Women With Osteoporosis or Osteopenia, Who Are GI Intolerant of Daily or Weekly Alendronate or Risendronate
Lead sponsor
Hoffmann-La Roche
Phase
Phase 4
Overall status
Completed
Start date
January 31, 2005
Completion date
September 30, 2006
Enrollment
545 (actual)
Sites
60

Conditions

As the registry lists them; a condition with its own page is linked.

postmenopausal osteoporosis