drugset / Trial / NCT02437890

A Phase II Study to Evaluate Safety and Efficacy of ALX-0061 in Subjects With Systemic Lupus Erythematosus

NCT02437890

Phase 2 Completed 312 enrolled Ablynx, a Sanofi company
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

EvaluationDrugModalityDoseRoute
Subject Vobarilizumab Protein / enzyme biologic 75 mg Subcutaneous
Subject Vobarilizumab Protein / enzyme biologic 150 mg Subcutaneous
Subject Vobarilizumab Protein / enzyme biologic 225 mg Subcutaneous