drugset / Trial / NCT00348296

Efficacy and Safety Study of GB-0998 for Treatment of Systemic Sclerosis

NCT00348296

Phase 3 Completed 60 enrolled Benesis Corporation
RandomizedParallel-groupDouble-blindTreatment

Summary

This randomized, double-blind, placebo-controlled multi-center study will carry out to assess the efficacy of GB-0998 in the treatment of the systemic sclerosis based on the changes in modified Rodnan total skin thickness score (TSS) as primary endopoint, and in addition, to assess the safety of GB-0998.

Timeline

Start
2006-07
Primary completion
2009-07
Completion
2009-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Immune Globulin Intravenous (Human) Protein / enzyme biologic 400 mg/kg

Indications