Acute Myeloid Leukemia Clinical Trial

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LCI-HEM-SPEC-001: Tissue Collection for Genetic Analysis of Acute Myelogenous Leukemia

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Summary

The purpose of this study is to obtain high quality specimens for molecular studies for the identification and characterization of genetic mutations involved in the pathogenesis of familial myeloid malignancies. Specimens obtained will be de-identified, linked to basic clinical data, and sent to Washington University (Division of Oncology, St. Louis, MO) for molecular analyses. Some specimens sent to Washington University may also be used for quality control analyses.

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Full Description

This is a specimen collection study for patients receiving standard of care treatment for AML. Specimens collected will be 1) bone marrow biopsy and aspiration, 2) peripheral blood, 3) skin punch biopsy, and 4) oral rinse. Collection of these specimens will be at timepoints determined by the patient's standard of care and their physician Investigator.

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Eligibility Criteria

Inclusion Criteria

Patients must have a diagnosis of acute myelogenous leukemia.
Family members of patients with acute myelogenous leukemia may be enrolled.
Informed consent must be provided by the patient or his/her legal guardian in accord with the practices of Levine Cancer Institute and Atrium Health.

Exclusion Criteria

Known infection with Hepatitis B or C, HTLV, or HIV.

Study is for people with:

Acute Myeloid Leukemia

Estimated Enrollment:

6

Study ID:

NCT01999556

Recruitment Status:

Completed

Sponsor:

Wake Forest University Health Sciences

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There is 1 Location for this study

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Levine Cancer Institute
Charlotte North Carolina, 28204, United States

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Study is for people with:

Acute Myeloid Leukemia

Estimated Enrollment:

6

Study ID:

NCT01999556

Recruitment Status:

Completed

Sponsor:


Wake Forest University Health Sciences

How clear is this clinincal trial information?

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