Overview

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

Status:
Completed
Trial end date:
2009-07-01
Target enrollment:
Participant gender:
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.
Phase:
Phase 3
Details
Lead Sponsor:
Benesis Corporation
Treatments:
Antibodies
gamma-Globulins
Immunoglobulins
Immunoglobulins, Intravenous
Rho(D) Immune Globulin