drugset / Trial / NCT01150890
Brodalumab (AMG 827) in Adults With Moderate to Severe Crohn's Disease
RandomizedParallel-groupDouble-blindTreatment
Summary
The study will examine the safety and effectiveness of brodalumab for the treatment of moderate to severe Crohn's disease. Participants will randomly assigned to receive either brodalumab or placebo (a lookalike liquid that doesn't have any drug in it) and neither the doctor nor the patient will know what treatment is being given.
Timeline
- Start
- 2010-11-09
- Primary completion
- 2011-10-15
- Completion
- 2011-10-15
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Brodalumab | Monoclonal antibody | 210 mg | Intravenous |
| Subject | Brodalumab | Monoclonal antibody | 350 mg | Intravenous |
| Subject | Brodalumab | Monoclonal antibody | 700 mg | Intravenous |