Clinical trial

A Research Study to Evaluate the Safety and Effectiveness of MK0217 to Prevent…

NCT00480766 · Organon and Co, Industry · Completed

Key facts

NCT number NCT00480766
Title A Research Study to Evaluate the Safety and Effectiveness of MK0217 to Prevent and Treat Bone Loss (0217-193)(COMPLETED)
Official title A Multicenter, Randomized, Double-Blind, Placebo-Controlled, 12-Month Study to Evaluate the Efficacy and Safety of Oral Alendronate Sodium Once Weekly for the Prevention and Treatment of Glucocorticoid-Induced Bone Loss
Lead sponsor Organon and Co, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Osteoporosis
Intervention type Drug
Interventions MK0217/Duration of Treatment : 12 Months
Enrollment 173
Start date Jul 1, 2001
Primary completion Aug 1, 2003
Completion Aug 1, 2003
First posted May 31, 2007
Last update posted Aug 14, 2024

At a glance

  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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