drugset / Trial / NCT00541658

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

NCT00541658

Phase 3 Completed 923 enrolled Warner Chilcott
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

EvaluationDrugModalityDoseRoute
Subject Risedronate Small molecule 5 mg Oral
Subject Risedronate Small molecule 35 mg Oral