drugset / Trial / NCT00885170

A Study to Evaluate the Safety, Tolerability, and Efficacy of Odanacatib (MK-0822) in Postmenopausal Women Previously Treated With a Bisphosphonate (MK-0822-042)

NCT00885170

Phase 2 Completed 246 enrolled Merck Sharp & Dohme LLC
RandomizedParallel-groupDouble-blindTreatment

Summary

The study will evaluate the both the efficacy of odanacatib on Bone Mineral Density (BMD) and the safety of odanacatib for postmenopausal osteoporosis in patients previously treated with alendronate. The primary hypothesis of the trial is that treatment with odanacatib 50 mg once weekly will increase bone mineral density at the femoral neck compared to placebo at the end of 24 months.

Timeline

Start
2009-04-13
Primary completion
2011-09-15
Completion
2011-09-15

Drugs

EvaluationDrugModalityDoseRoute
Subject Odanacatib Small molecule 50 mg

Indications