Viewing Study NCT00502112



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Last Modification Date: 2024-10-26 @ 9:34 AM
Study NCT ID: NCT00502112
Status: COMPLETED
Last Update Posted: 2011-10-12
First Post: 2007-07-13

Brief Title: A Phase I Study of Lintuzumab Combined With Lenalidomide in Patients With Myelodysplastic Syndromes MDS
Sponsor: Seagen Inc
Organization: Seagen Inc

Study Overview

Official Title: A Phase I Combination Trial of SGN-33 Anti-huCD33 mAb HuM195 Lintuzumab and Lenalidomide Revlimid in Patients With Myelodysplastic Syndromes MDS
Status: COMPLETED
Status Verified Date: 2011-10
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
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: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None