drugset / Trial / NCT01635621
A Phase II Study to Assess the Efficacy and Safety of Olokizumab in Patients With Crohn's Disease
RandomizedParallel-groupDouble-blindTreatment
Summary
The primary purpose of this multi-centre, double blind-study is to evaluate the clinical response of patients with moderate to severe Cohn's Disease (CD) following treatment with different doses and dose regimens of Olokizumab, relative to placebo.
Timeline
- Start
- 2012-06
- Primary completion
- 2013-08
- Completion
- 2013-08
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Olokizumab | Monoclonal antibody | 120 mg | Subcutaneous |
| Subject | Olokizumab | Monoclonal antibody | 240 mg | Subcutaneous |