drugset / Trial / NCT00888745

A Study of the Safety and Pharmacokinetics of PRO283698 in Patients With Rheumatoid Arthritis

NCT00888745

Phase 1 Completed 65 enrolled Genentech, Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

This is a Phase I multicenter study that will be conducted in the United States and Europe.

Timeline

Start
2009-05
Primary completion
2010-06
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject pateclizumab Monoclonal antibody 0.3 mg/kg Intravenous
Subject pateclizumab Monoclonal antibody 1 mg/kg Intravenous
Subject pateclizumab Monoclonal antibody 3 mg/kg Intravenous
Subject pateclizumab Monoclonal antibody 5 mg/kg Intravenous

Indications