drugset / Trial / NCT02529956
A Study to Assess the Safety, Pharmacokinetics and Pharmacodynamics of UCB4940 in Patients With Psoriasis
RandomizedParallel-groupDouble-blindTreatment
Summary
To evaluate the safety of UCB4940 administered by iv infusion of a single ascending dose in subjects with mild to moderate plaque psoriasis.
Timeline
- Start
- 2012-11
- Primary completion
- 2014-01
- Completion
- 2014-01
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Bimekizumab | Monoclonal antibody | 8 mg | Intravenous |
| Subject | Bimekizumab | Monoclonal antibody | 40 mg | Intravenous |
| Subject | Bimekizumab | Monoclonal antibody | 160 mg | Intravenous |
| Subject | Bimekizumab | Monoclonal antibody | 480 mg | Intravenous |
| Subject | Bimekizumab | Monoclonal antibody | 640 mg | Intravenous |