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Brief Title: A Phase I Study of Lintuzumab Combined With Lenalidomide in Patients With Myelodysplastic Syndromes (MDS)
Official Title: A Phase I Combination Trial of SGN-33 (Anti-huCD33 mAb; HuM195; Lintuzumab) and Lenalidomide (Revlimid®) in Patients With Myelodysplastic Syndromes (MDS)
Study ID: NCT00502112
Brief 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.
Detailed Description:
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
University of Alabama at Birmingham, Birmingham, Alabama, United States
Rocky Mountain Cancer Center, Denver, Colorado, United States
Georgetown University, Washington, District of Columbia, United States
Georgia Cancer Specialists, Atlanta, Georgia, United States
St.Vincent's Comprehensive Cancer Center, New York, New York, United States
Memorial Sloan-Kettering Cancer Center, New York, New York, United States
Ohio State University, Columbus, Ohio, United States
Avera Cancer Institute, Sioux Falls, South Dakota, United States
Name: Eric Sievers, MD
Affiliation: Seagen Inc.
Role: STUDY_DIRECTOR