COVID-19 vaccination in patients with classic and variant hairy cell leukemia.
Robert J Kreitman, Lacey James, Julie Feurtado...
https://pubmed.ncbi.nlm.nih.gov/40552139Actively Recruiting
Led by National Cancer Institute (NCI) · Updated on 2026-06-05
1263
Participants Needed
1
Research Sites
N/A
Total Duration
Researchers are studying hairy cell leukemia (HCL) and other blood and lymphatic system cancers to better understand these diseases and how they compare to each other and to healthy individuals. They are particularly interested in developing new treatments using recombinant immunotoxins, which are antibodies attached to toxins that target and kill cancer cells. This observational study collects clinical samples from patients with leukemia or other cancers and from healthy volunteers to support this research. Participants with leukemia or other cancers will provide blood, bone marrow, urine, and tumor tissue samples as requested by the researchers. Healthy volunteers will provide blood and urine samples only. No treatments are given as part of this study. Samples may be collected before or after treatments, during disease assessments, or at times of response or relapse. Collection can occur at the research center or local providers and sent to the study site. The study also includes ongoing follow-up for participants with hairy cell leukemia, especially those who have completed prior treatments. During the study, participants will provide various biological samples and clinical data to help researchers analyze disease processes and treatment effects. Researchers will obtain tissue samples within four weeks and follow up with hairy cell leukemia participants approximately every two years. The study involves informed consent and does not provide experimental treatment but supports understanding of leukemia and related cancers to improve future therapies. Participation duration varies based on individual disease status and follow-up schedules.
CONDITIONS
Collection of Human Samples to Study Hairy Cell and Other Leukemias, and to Develop Recombinant Immunotoxins for Cancer Treatment
You may qualify if you...
You will not qualify if you...
Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person) for informed consent and initial eligibility assessment
Duration - Up to 4 weeks
Participants provide biological samples such as blood, tumor, and other tissues for research purposes. Samples may be collected prior to or after treatment, during disease assessments, and at times of response or relapse.
1 or more visits depending on sample availability and timing
Duration - Approximately every 2 years
Participants, especially those with hairy cell leukemia, are followed systematically to observe disease status and collect data over time.
Follow-up visits about every 2 years
Total: 1 location
1
National Institutes of Health Clinical Center
Bethesda, Maryland, United States, 20892
Actively Recruiting
J
Julie C Feurtado, R.N.
R
Robert J Kreitman, M.D.
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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