A Study of a 35 mg Delayed Release Formulation of Risedronate for Osteoporosis

Update Il y a 4 ans
Reference: NCT00541658

Woman Man

Extract

The purpose of this trial is to study the efficacy of a 35 mg delayed release weekly dosing regimen as compared to the standard daily dosing regimen of risedronate 5 mg daily.


Inclusion criteria

  • Postmenopausal osteoporosis


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