Clinical

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Study of the Monoclonal Antibody IMT-009 in Patients With Advanced Solid Tumors or Lymphomas


ABSTRACT: This is a Phase 1/2a open-label, multicenter, dose escalation and dose expansion trial in which IMT-009 will be administered by the intravenous (IV) route to participants with solid tumors or lymphomas. The main goals of this study are to: * Find the recommended dose of IMT-009 that can be safely given to participants * Learn more about the side effects of IMT-009 * Learn more about pharmacokinetics of IMT-009 * Learn more about the effectiveness of IMT-009 * Learn more about different pharmacokinetic biomarkers and how they might change in the presence of IMT-009

DISEASE(S): Lymphoma, Large B-cell, Diffuse,Carcinoma,Triple Negative Breast Neoplasms,Hodgkin Disease,Colorectal Cancer,Non Small Cell Lung Cancer,Triple Negative Breast Cancer,Hormone Receptor Positive Breast Carcinoma,Breast Neoplasms,Cutaneous Squamous Cell Carcinoma,Small Bowel Cancer,Hodgkin Lymphoma,Esophageal Neoplasms,Colorectal Neoplasms,Carcinoma, Non-small-cell Lung,Head And Neck Squamous Cell Carcinoma,Lymphoma, T-cell,Lymphoma, T-cell, Peripheral,Solid Tumor,Diffuse Large B Cell Lymphoma,Burkitt Lymphoma,Diffuse Large B-cell Lymphoma,Lymphoma,Carcinoma, Squamous Cell,Squamous Cell Carcinoma Of Head And Neck,T-cell Lymphoma,Esophageal Cancer,Lymphoma, B-cell

PROVIDER: 2750284 | ecrin-mdr-crc |

REPOSITORIES: ECRIN MDR

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