drugset / Trial / NCT00715676

Phase 2 Safety and Efficacy Study of a Vitamin D Compound (DP001) in Postmenopausal Women With Low Bone Mineral Density

NCT00715676

Phase 2 Completed 157 enrolled Deltanoid Pharmaceuticals
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study will evaluate the effect of a 1-year administration of the vitamin D analog 2-methylene-19-nor-(20S)-1alpha, 25-dihydroxyvitamin D3 (DP001) on bone mineral density (BMD), safety, and tolerability.

Timeline

Start
2007-03
Primary completion
2008-12
Completion
2009-01

Drugs

EvaluationDrugModalityDoseRoute
Subject DP001 Small molecule 220 ng Oral
Subject DP001 Small molecule 440 ng Oral

Indications