Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
ID01087333

Study of Hairy Cell and Other Leukemias Focusing on Recombinant Immunotoxins for Cancer Treatment

Led by National Cancer Institute (NCI) · Updated on 2026-06-05

1263

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

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

Brief Title

Collection of Human Samples to Study Hairy Cell and Other Leukemias, and to Develop Recombinant Immunotoxins for Cancer Treatment

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • 18 years of age and older
  • Willingness to provide data and biological samples for research
  • Ability to understand and sign informed consent
  • Diagnosis of hematologic malignancy or solid tumor, including those in long-term remission
  • Normal donors must have no current or prior diagnosis of cancer
Not Eligible

You will not qualify if you...

  • Known pregnancy at the time of enrollment
  • Pregnancy test required before any research procedure involving more than minimal risk

AI-Screening

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Your Study Journey

Screening

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

Sample Collection

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

Long-term Monitoring

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

Trial Site Locations

Total: 1 location

1

National Institutes of Health Clinical Center

Bethesda, Maryland, United States, 20892

Actively Recruiting

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Research Team

J

Julie C Feurtado, R.N.

R

Robert J Kreitman, M.D.

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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Published Research Related To This Trial

Characterization of B-cell receptor clonality and immunoglobulin gene usage at multiple time points during active SARS-CoV-2 infection.

Evgeny Arons, Kiersten Henry, Christopher Haas...

https://pubmed.ncbi.nlm.nih.gov/37877800