drugset / Trial / NCT00502112

A Phase I Study of Lintuzumab Combined With Lenalidomide in Patients With Myelodysplastic Syndromes (MDS)

NCT00502112

Phase 1 Completed 13 enrolled Seagen Inc.
NaSingle-groupOpen-labelTreatment

Summary

This study is a phase I, open-label, single-arm, dose escalation trial to determine the safety and activity of lenalidomide combined with lintuzumab in patients with MDS. Small groups of 3-6 patients will be treated with pre-specified doses of lenalidomide and lintuzumab and will receive 3-week cycles of combination therapy.

Timeline

Start
2008-03
Primary completion
2010-05
Completion
2010-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Lenalidomide Other / unclassified 10 mg Oral
Subject Lenalidomide Other / unclassified 15 mg Oral
Subject lintuzumab Monoclonal antibody 4 mg/kg Intravenous
Subject lintuzumab Monoclonal antibody 8 mg/kg Intravenous