drugset / Trial / NCT00103779

A Safety Study of SGN-40 in Patients With Non-Hodgkin's Lymphoma

NCT00103779

Phase 1 Completed 50 enrolled Seagen Inc. Genentech, Inc. · collab
NaSingle-groupOpen-labelTreatment

Summary

This is an open-label, multi-dose, Phase I, dose escalation study to define the safety profile and preliminary anti-tumor activity of SGN-40 in patients with refractory or recurrent non-Hodgkin B-cell lymphomas.

Timeline

Start
2004-12
Primary completion
2007-03
Completion
2007-03

Drugs

EvaluationDrugModalityDoseRoute
Subject dacetuzumab Monoclonal antibody 1 mg/kg Intravenous
Subject dacetuzumab Monoclonal antibody 2 mg/kg Intravenous
Subject dacetuzumab Monoclonal antibody 3 mg/kg Intravenous
Subject dacetuzumab Monoclonal antibody 4 mg/kg Intravenous
Subject dacetuzumab Monoclonal antibody 8 mg/kg Intravenous

Indications