drugset / Trial / NCT02514967
CHABLIS7.5: A Study of the Efficacy and Safety of Subcutaneous Blisibimod in Subjects With Systemic Lupus Erythematosus With or Without Nephritis
RandomizedParallel-groupQuadruple-blindTreatment
Summary
The purpose of this study is to evaluate the clinical efficacy of blisibimod as measured by a composite responder index in subjects who, despite corticosteroid use, continue to have seropositive, clinically-active Systemic Lupus Erythematosus (SLE) as defined by SELENA-SLEDAI score ≥10, and positive for anti-double stranded DNA and low complement (C3 or C4).
Timeline
- Start
- 2016-06
- Primary completion
- 2016-11
- Completion
- 2017-02-28
Outcome
Outcome not reported
Stopped: “Study halted prematurely and will not resume. Subjects were seen until February 2017”
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Blisibimod | Peptide | — | Subcutaneous |