The purpose of this study is to evaluate treatment adherence to different regimens of ibandronate in postmenopausal women with osteoporosis or osteopenia who are intolerant to daily or weekly alendronate or risedronate therapy due to gastrointestinal (GI) side effects. The anticipated time on study treatment is 12 months, and the target sample size is 517 individuals.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
545
Either 150 mg oral tablet once monthly or 3 mg IV injection once every 3 months
Percentage of participants who have greater than or equal to (>=) 75 percent (%) adherence using either monthly oral ibandronate or quarterly intravenous (IV) ibandronate
Time frame: 12 months
Percentage of participants who have an adherence of >= 75% using ibandronate including both switch and non-switch participants
Time frame: 12 months
Percentage of participants with GI events based on severity
Time frame: Up to 10 months
Percentage of participants who experienced a change in frequency and number of GI events
Time frame: Up to 10 months
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Montgomery, Alabama, United States
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Lake Havasu City, Arizona, United States
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Paradise Valley, Arizona, United States
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Pine Bluff, Arkansas, United States
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San Diego, California, United States
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San Diego, California, United States
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Santa Monica, California, United States
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Vista, California, United States
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Beverly Hills, Florida, United States
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