Actively Recruiting

Age: 30Years +
All Genders
Healthy Volunteers
NCT06644625

CHAAMP (CHArlotte Advocate MGUS Project) Internal Pilot Study

Led by Wake Forest University Health Sciences · Updated on 2026-01-20

1665

Participants Needed

1

Research Sites

513 weeks

Total Duration

On this page

Sponsors

W

Wake Forest University Health Sciences

Lead Sponsor

A

Atrium Health Levine Cancer Institute

Collaborating Sponsor

AI-Summary

What this Trial Is About

The purpose of this study is to identify multiple myeloma in the precancerous MGUS stage in order to reduce the risk of delayed diagnosis of multiple myeloma, decrease morbidity related to multiple myeloma at progression, and improve long term outcomes.

CONDITIONS

Official Title

CHAAMP (CHArlotte Advocate MGUS Project) Internal Pilot Study

Who Can Participate

Age: 30Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 30 years or older at the time of consent
  • Self-identify as Black and/or African American OR be a first-degree relative of a patient diagnosed with a plasma cell disorder
  • Capable and willing to provide informed consent
  • Reside in Charlotte, NC, or the surrounding area
  • Test positive for monoclonal gammopathy during screening to join the longitudinal study
  • Consent to participate in the longitudinal portion of the study
Not Eligible

You will not qualify if you...

  • History of MGUS, smoldering multiple myeloma, multiple myeloma, AL amyloidosis, plasma cell leukemia, solitary plasmacytoma, Waldenstrom Macroglobulinemia, or POEMS syndrome
  • Previously underwent diagnostic workup in this study without a diagnosis of MGUS, smoldering multiple myeloma, or other non-plasma cell disorder

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Atrium Health Levine Cancer

Charlotte, North Carolina, United States, 28204

Actively Recruiting

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Research Team

M

Margarita Dzhanumova

CONTACT

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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