drugset / Trial / NCT00648739

Safety and Dose Ranging Study of Samalizumab to Treat Relapsing or Refractory CLL or MM

NCT00648739

Phase 1/2 Terminated 26 enrolled Alexion Pharmaceuticals, Inc.
SequentialOpen-labelTreatment

Summary

The purpose of this study was to determine the safety and maximum tolerated dose (MTD) of ALXN6000 (samalizumab) in treating relapsing or refractory B-cell chronic lymphocytic leukemia (B-CLL) or multiple myeloma (MM) and to study how samalizumab may help the immune system fight tumors that express CD200.

Timeline

Start
2008-06-19
Primary completion
2010-12-14
Completion
2010-12-14

Drugs

EvaluationDrugModalityDoseRoute
Subject Samalizumab Monoclonal antibody 50 mg/m2 Intravenous
Subject Samalizumab Monoclonal antibody 600 mg/m2 Intravenous