Identifying precancerous multiple myeloma in African American adults
Official title: CHAAMP (CHArlotte Advocate MGUS Project) Internal Pilot Study
Run by Wake Forest University Health Sciences · NCT06644625 · Data updated 2026-11-12
This study is testing a way to find early signs of multiple myeloma in Black and African American adults aged 30 and older to help catch it sooner and improve their health outcomes.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 30 Years and up |
| Sex | All |
| Enrollment | 1665 (estimated) |
| Sponsor | Wake Forest University Health Sciences Academic / other |
| Locations | 1 site (Charlotte, North Carolina) |
| Status | Recruiting |
| Started | March 1, 2025 |
| Main results expected | January 2035 |
| Study ends | January 2035 |
| Registry record updated | July 13, 2026 |
| Trial ID | NCT06644625 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are Black and/or African American adults aged 30 years or older living in Charlotte, NC, who are willing to participate in screening.
✕Probably not a fit
Patients with a self-reported history of MGUS, smoldering multiple myeloma, or other related plasma cell disorders will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
The CHAAMP Internal Pilot aims to identify multiple myeloma at the precancerous stage of monoclonal gammopathy of undetermined significance (MGUS) in Black and/or African American adults aged 30 and older. Over a one-year period, participants residing in Charlotte, NC, will be screened for MGUS, with a target enrollment of 1665 individuals. Those who test positive will receive referrals for further diagnostic evaluation and may consent to a longitudinal follow-up for up to 10 years. The study seeks to reduce the risk of delayed diagnosis and improve long-term outcomes for participants.
Why it matters
Potential benefit: If successful, this study could lead to earlier detection and better management of multiple myeloma, ultimately improving patient outcomes.
How similar studies have gone: Other studies have shown success in early detection of multiple myeloma through screening, making this approach promising.
Who can join: the full rules
Show full inclusion / exclusion criteria
SCREENING Inclusion Criteria: * Age 30 years or older at the time of consent * Either: 1. Self-identify as Black and/or African American OR 2. First-degree relatives (parents, siblings, or children) of patients of any race or ethnicity diagnosed with a plasma cell disorder, including MGUS, smoldering multiple myeloma (SMM), multiple myeloma (MM), solitary plasmacytoma, plasma cell leukemia, AL amyloidosis, POEMS syndrome, and Waldenström's Macroglobulinemia * Capable and willing to provide informed consent. NOTE: HIPAA (Health Insurance Portability and Accountability Act) authorization for the release of personal health information may be included in the informed consent or obtained separately * Reside in Charlotte, NC, or the surrounding area, based on self-report SCREENING Exclusion Criteria: * Self-reported history of MGUS, SMM, MM, AL amyloidosis, plasma cell leukemia, solitary plasmacytoma, Waldenstrom Macroglobulinemia, and POEMS. LONGITUDINAL Inclusion Criteria: * Test positive for monoclonal gammopathy during screening portion of the study * Consent to the longitudinal portion of the study LONGITUDINAL Exclusion Criteria: * The participant previously underwent diagnostic work up as part of CHAAMP Internal Pilot that did not result in a diagnosis of MGUS, Smoldering Multiple Myeloma or other non-plasma cell disorder.
Where it's running
-
Atrium Health Levine Cancer
Charlotte, North Carolina, United States Recruiting
Study contacts
- Principal investigator: Manisha Bhutani, MD — Atrium Health Wake Forest Baptist Comprehensive Cancer Center
- Study coordinator: Margarita Dzhanumova
- Email: margarita.dzhanumova@atriumhealth.org
- Phone: 704-754-3768
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Multi-omics profiling to predict progression from MGUS and smoldering myeloma to symptomatic multiple myeloma
This project will try to see if combined genomic, immune, and oral microbiome tests can predict which people with MGUS or smoldering myeloma will progress to symptomatic multiple myeloma.
-
Sequential CAR-T therapy targeting BCMA and GPRC5D for relapsed or refractory multiple myeloma
This will try sequential CAR-T cell therapy against BCMA and GPRC5D in people with relapsed or refractory multiple myeloma to see if it is safe and helps control the disease.
-
Analyzing gut microbiota in patients with monoclonal gammopathy
This study is trying to see how the gut bacteria of people with monoclonal gammopathy differ from those without the condition to help find new ways to diagnose and treat it.
-
Early palliative care for patients with multiple myeloma and aggressive lymphoma
This study is testing if early palliative care can improve the quality of life and comfort for people with multiple myeloma and aggressive lymphoma while they receive their usual cancer treatment.
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Testing linvoseltamab for eliminating abnormal plasma cells in patients with high-risk MGUS or smoldering multiple myeloma
This study is testing if a new drug called linvoseltamab can help get rid of abnormal plasma cells in patients with high-risk MGUS or smoldering multiple myeloma.
-
Cohort of patients with plasma cell disorders at Peking University First Hospital
This study is looking at hospitalized patients with plasma cell disorders to see how their treatment and disease status affect their outcomes over time.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.