drugset / Trial / NCT02437890
A Phase II Study to Evaluate Safety and Efficacy of ALX-0061 in Subjects With Systemic Lupus Erythematosus
RandomizedParallel-groupQuadruple-blindTreatment
Summary
Primary objective: To assess the efficacy and safety of different dose regimens of ALX-0061 administered subcutaneously (s.c.) to subjects with moderate to severe active, seropositive systemic lupus erythematosus (SLE) compared to placebo. Secondary objectives: To assess the pharmacokinetics (PK), pharmacodynamics (PD), immunogenicity, flare rate, steroid reduction and health-related quality of life, with different dose regimens of ALX-0061.
Timeline
- Start
- 2015-07
- Primary completion
- 2018-01
- Completion
- 2018-01
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Vobarilizumab | Protein / enzyme biologic | 75 mg | Subcutaneous |
| Subject | Vobarilizumab | Protein / enzyme biologic | 150 mg | Subcutaneous |
| Subject | Vobarilizumab | Protein / enzyme biologic | 225 mg | Subcutaneous |