drugset / Trial / NCT00390091

Study of LJP 394 (Abetimus Sodium) in Lupus Patients

NCT00390091 ↗

RandomizedParallel-groupSingle-blindDiagnostic

Summary

The primary purpose of this study is to assess the safety and pharmacodynamic effect of LJP 394 at doses of 100 mg, 300 mg and 900 mg on anti-dsDNA antibody levels in patients with SLE.

Timeline

Start
2006-09
Primary completion
—
Completion
—

Drugs

EvaluationDrugModalityDoseRoute
Subject Abetimus Unknown 100 mg —
Subject Abetimus Unknown 300 mg —
Subject Abetimus Unknown 900 mg —