Non Hodgkin Lymphoma Clinical Trial
Immunogenicity and Safety of Commercially Available Vaccines Against SARS-CoV-2 (COVID-19) in Patients With Hematologic Malignancies
Summary
D1. Primary Objective:
1. Determine the immunogenicity of FDA approved COVID-19 vaccination in patients with hematologic malignancies
D2. Secondary Objectives:
Assess the safety of FDA approved COVID-19 vaccination in patients with hematologic malignancies
Analyze the kinetics of immunogenic response over time after receipt of the COVID-19 vaccination
Compare the immunogenicity of different COVID-19 vaccinations that will be approved by the FDA
Analyze advanced flow immunophenotyping of innate and adaptive immune blood cells in all participants and correlate with response to vaccination
Eligibility Criteria
Inclusion Criteria:
Patients must not have received any prior COVID-19 vaccination
Patients must have any one of the following diagnosis:
a. Monoclonal B-cell lymphocytosis b. Chronic lymphocytic leukemia/small lymphocytic lymphoma c. B-cell Non-Hodgkin's lymphoma: i. Follicular lymphoma ii. Mantle cell lymphoma iii. Diffuse large B-cell lymphoma iv. Marginal zone lymphoma v. Burkitt lymphoma vi. Double hit/triple hit lymphoma vii. Lymphoplasmacytic lymphoma/Waldenstrom's macroglobulinemia d. Hodgkin lymphoma
Exclusion Criteria:
Receipt of any vaccination (e.g., influenza, recombinant zoster) 2 weeks prior to registration
Prior chemotherapy, immunotherapy or oral agent therapy that was completed >12 months prior to enrollment. NOTE: patients who are on oral agents for the treatment of their underlying malignancy will be allowed. Some of these medication classes include Bruton tyrosine kinase inhibitor (BTKi), BCL2 antagonists, PI3 kinase inhibitors, immunomodulatory agents, among others. Please contact the Principal Investigator for any clarification about these medications.
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There is 1 Location for this study
Rochester Minnesota, 55902, United States
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