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The primary objective of this trial is to estimate efficacy of the novel regimen. The primary endpoint is the 1-year PFS rate after treatment with one dose of pembrolizumab followed by four to six cyc...
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Lead Sponsor
University of Cologne
NCT07249528 · Non-hodgkin Lymphoma, Multiple Myeloma
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1st Department of Medicine, Cologne University Hospital
Cologne
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This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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