Bisphosphonate Treatment of Osteogenesis Imperfecta
Completed · Phase 2
Conditions studied: Osteogenesis Imperfecta
In brief
The primary purpose of this trial is to evaluate whether the investigational medication is safe, effective and has the ability to increase spine bone density in osteogenesis imperfecta (OI) patients.
Key facts
- Study ID
- NCT00063479
- Run by
- Novartis Pharmaceuticals
- People needed
- 158
- Starts
- 2003-06-01
- Expected to finish
- 2007-05-01
- Last updated by the study team
- 2017-06-01
Who can join
Age: 0 and older, up to 17. Sex: any. Healthy volunteers: not accepted.
Where it is running
- UCLA - Division of Pediatric Nephrology — Los Angeles, California, United States
- Alfred I. DuPont Hospital for Children — Wilmington, Delaware, United States
- Intermountain Orthopedics — Boise, Idaho, United States
- St. Jude Children's Research Hospital — Peoria, Illinois, United States
- Children's Hospital — Omaha, Nebraska, United States
- Children's Hospital Medical Center — Cincinnati, Ohio, United States
- Children's Hospital — Columbus, Ohio, United States
- Oregon Health Sciences University — Portland, Oregon, United States
- Vanderbilt University Medical Center — Nashville, Tennessee, United States
- Texas Children's Hosptial — Houston, Texas, United States
Full record on ClinicalTrials.gov
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