drugset / Trial / NCT00541658
A Study of a 35 mg Delayed Release Formulation of Risedronate for Osteoporosis
RandomizedParallel-groupTriple-blindTreatment
Summary
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.
Timeline
- Start
- 2007-10
- Primary completion
- 2010-04
- Completion
- 2010-04
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Risedronate | Small molecule | 5 mg | Oral |
| Subject | Risedronate | Small molecule | 35 mg | Oral |