drugset / Trial / NCT00632216

A Study to Determine the Satisfaction With Actonel in Postmenopausal Women With Osteoporosis

NCT00632216

Phase 4 Completed 464 enrolled Sanofi
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The study in the labeled and real conditions of prescription of Actonel will investigate the satisfaction of patients with its new formulation: 35 mg Once A Week. The study will also measure response rates in CTX (the C-telopeptide of type I collagen) at baseline and after 12 weeks of treatment with risedronate 35 mg Once A Week.

Timeline

Start
2004-05
Primary completion
Completion
2006-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Risedronate Small molecule 35 mg