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Clinical Trial Summary

The purpose of this study is to evaluate the safety, pharmacokinetics, immunogenicity, and efficacy of zilovertamab vedotin given intravenously (IV) across a range of dose levels in participants with previously treated hematological cancers including acute lymphocytic leukemia (ALL), acute myeloid leukemia (AML), Burkitt lymphoma (BL), chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL), diffuse large B-cell lymphoma (DLBCL), follicular lymphoma (FL), lymphoplasmacytoid lymphoma/Waldenström macroglobulinemia (LPL/WM), mantle cell lymphoma (MCL), marginal zone lymphoma (MZL), Richter transformation lymphoma (RTL), and T-cell non-Hodgkin lymphoma (NHL).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03833180
Study type Interventional
Source VelosBio Inc., a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA)
Contact
Status Completed
Phase Phase 1
Start date March 14, 2019
Completion date December 18, 2023

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