drugset / Trial / NCT00453492

Risedronate Sodium in Post Menopausal Osteoporosis

NCT00453492

Phase 4 Completed 246 enrolled Sanofi Procter and Gamble · collab
RandomizedCrossoverOpen-labelTreatment

Summary

The primary objective is to compare subject satisfaction of once a week dosing of 35 mg Actonel to once daily dosing of 5 mg Actonel in postmenopausal osteoporotic women. The secondary objectives are to measure compliance (50 % drug taken), and persistence, \[and urinary NTx (N-telopeptides) (optional)\].

Timeline

Start
2004-01
Primary completion
Completion

Drugs

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