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

NCT02514967 ↗

Phase 3 Terminated 3 enrolled Anthera Pharmaceuticals
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

EvaluationDrugModalityDoseRoute
Subject Blisibimod Peptide — Subcutaneous