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Assess the Influence of a High-fat Meal on the Relative Bioavailability Of Two Formulations of Risedronate
This is a randomized, open-label, multi-center, 4-treatment, 4-period crossover study. Approximately 72 healthy, surgically sterile or postmenopausal subjects will be enrolled and have urine collected over 72 hours following administration of risedronate for all 4 treatment periods).
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