drugset / Trial / NCT00259857
Safety and Efficacy of Alendronate (Fosamax) in Children With Osteoporosis
Phase 2
Completed
22 enrolled
Medical University of South Carolina
FDA Office of Orphan Products Development · collabMerck Sharp & Dohme LLC · collab
RandomizedCrossoverDouble-blindTreatment
Summary
We have previously evaluated the safety and efficacy of Alendronate in 10 patients with juvenile osteoporosis during a 12-month clinical trial. We have documented that Alendronate improved BMD of the spine and hip without any major side effects. There were no additional fractures during therapy. The present study is designed to further evaluate the safety and efficacy of Alendronate in 20 children with juvenile osteoporosis using a double-blind, randomized, placebo-controlled, cross-over protocol.
Timeline
- Start
- 2003-10
- Primary completion
- 2008-03
- Completion
- 2009-08
Publications
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Alendronic Acid | Small molecule | 35 mg | Oral |
| Subject | Alendronic Acid | Small molecule | 70 mg | Oral |