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RECRUITINGOBSERVATIONAL

Predicting Progression of Developing Myeloma in a High-Risk Screened Population and General Population

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

We will seek consent from participants to use the data and biospecimens collected according study protocol to address additional research questions for MGUS, SMM, MM, and other conditions. Our overarching hypothesis is that early detection of MGUS/SMM in a high- risk population, along with the comprehensive characterization of genomic/epigenomic and microenvironmental/immune regulators of disease progression will lead to strategies that intercept disease progression and improve survival.

Who May Be Eligible (Plain English)

Who May Qualify: - Must meet criteria of the high-risk population as described with one of the below criteria - ≥ 30 years AND - first-degree relative of a patient with a plasma cell dyscrasia such as MGUS, SMM, MM, and Waldenström's Macroglobulinemia, or another blood cancer. OR - Age ≥ 18 years with 2 or more first- or second-degree relatives with a plasma cell dyscrasia such as MGUS, SMM, MM, and Waldenström's Macroglobulinemia, or another blood cancer ' - Voluntary written willing to sign a consent form must be given with the understanding that consent may be withdrawn by the patient at any time without prejudice to future medical care Who Should NOT Join This Trial: - • Persons diagnosed with cancer at any site (including hematologic cancers) with symptomatic disease requiring active therapy. - Persons with an already diagnosed plasma cell dyscrasia such as MGUS, SMM, MM, and Waldenström's Macroglobulinemia - Female patient who have a positive serum pregnancy test during the screening period or a positive pregnancy test. Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: * Must meet criteria of the high-risk population as described with one of the below criteria * ≥ 30 years AND * first-degree relative of a patient with a plasma cell dyscrasia such as MGUS, SMM, MM, and Waldenström's Macroglobulinemia, or another blood cancer. OR * Age ≥ 18 years with 2 or more first- or second-degree relatives with a plasma cell dyscrasia such as MGUS, SMM, MM, and Waldenström's Macroglobulinemia, or another blood cancer ' * Voluntary written informed consent must be given with the understanding that consent may be withdrawn by the patient at any time without prejudice to future medical care Exclusion Criteria: * • Persons diagnosed with cancer at any site (including hematologic cancers) with symptomatic disease requiring active therapy. * Persons with an already diagnosed plasma cell dyscrasia such as MGUS, SMM, MM, and Waldenström's Macroglobulinemia * Female patient who have a positive serum pregnancy test during the screening period or a positive pregnancy test.

Treatments Being Tested

DIAGNOSTIC_TEST

blood sampling

Participants will provide a blood sample that will be used to determine whether they have a monoclonal protein

Locations (3)

Soroka
Beersheba, Israel
Rabin medical center
Petah Tikva, Israel
TASMC
Tel Aviv, Israel