Clinical trial Recruiting at 1 site Observational Ages 21 and up

Understanding and Addressing Multiple Myeloma Disparities

Official title: Development of a Research Infrastructure for Understanding and Addressing Multiple Myeloma Disparities

Run by University of California, Davis · NCT04314752 · Data updated 2026-11-12

This study is trying to find better ways to recruit and survey patients from different backgrounds who have Multiple Myeloma to understand how it affects them and improve their care.

Quick facts

Study typeObservational
Ages21 Years and up
SexAll
Enrollment4000 (estimated)
SponsorUniversity of California, Davis
Academic / other
Locations1 site (Sacramento, California)
StatusRecruiting
StartedSeptember 1, 2020
Main results expectedDecember 30, 2026
Study endsDecember 30, 2026
Registry record updatedSeptember 14, 2026
Trial IDNCT04314752 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include adults aged 21 and older who have been diagnosed with Multiple Myeloma within the last five years and identify as African American, Latino, Asian American, Native Hawaiian, Pacific Islander, or non-Hispanic White.

Probably not a fit

Patients who do not have a diagnosis of Multiple Myeloma or are under the age of 21 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

This study aims to develop and evaluate protocols for conducting research focused on ethnic and racial minorities affected by Multiple Myeloma (MM) using cancer registry data. The investigators will identify, recruit, and survey patients from diverse backgrounds, including African Americans, Latinos, Asian Americans, Native Hawaiians, Pacific Islanders, and non-Hispanic Whites, to gather information on factors related to MM etiology and survival. Initially, a pilot phase will contact 400 eligible patients to assess the feasibility of the recruitment and survey process, with plans to expand to a larger cohort of 1,000 patients per ethnic group across California. The ultimate goal is to inform best practices for recruiting minority populations and to lay the groundwork for larger studies on MM.

Why it matters

Potential benefit: If successful, this study could lead to improved understanding and treatment strategies for Multiple Myeloma in minority populations.

How similar studies have gone: While this approach is focused on minority disparities in Multiple Myeloma, similar studies have shown success in addressing health disparities in other cancer types.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Diagnosed with a first primary pathologically confirmed case of Multiple Myeloma within the previous 5 years
* At least 21 years of age at the time of diagnosis
* Must have been diagnosed in one of the 48 counties in California
* Participant must be alive
* Identify as one of the following: African American, Latino, Asian American/Native Hawaiian/Pacific Islander, Non-Hispanic White

Exclusion Criteria:

* People who have not been diagnosed with Multiple Myeloma
* Under the age of 21
* Pregnant
* Prisoner

Where it's running

  • University of California Davis Comprehensive Cancer Center
    Sacramento, California, United States
    Recruiting

Study contacts

  • Principal investigator: Luis Carvajal-Carmona, PhD — University of California, Davis
  • Study coordinator: Luis Carvajal-Carmona, PhD
  • Email: lgcarvajal@ucdavis.edu
  • Phone: 5307529654

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.