NIH-funded research R37 grant

Identifying genetic markers to distinguish between benign and malignant myeloma precursor conditions

Official title: Myeloma Defining Genomic Events to Differentiate Benign and Malignant Myeloma Precursor Conditions

Funded at University of Miami School of Medicine · NIH-11050304 · Data updated 2026-11-12

This study is looking at the genetic changes that can help tell if someone with a benign condition related to multiple myeloma might develop the disease, so we can find out who is at higher risk and help them sooner.

More Myeloma research and trials

Quick facts

Grant typeR37 grant
Study typeNIH-funded research
Funding institutionUniversity of Miami School of Medicine
NIH-funded
Lab location1 site (Coral Gables, United States)
Project startFebruary 3, 2025
Project endJanuary 31, 2030
Funding year2025
Award (this year)$674,440
NIH project number1R37CA289752-01A1
Project IDNIH-11050304 on NIH RePORTER

Who could benefit from this research

Could help

Ideal candidates for this research include adults diagnosed with benign monoclonal gammopathy or smoldering myeloma who are at risk of progression to multiple myeloma.

Less likely to help

Patients who have already been diagnosed with symptomatic multiple myeloma or those without any precursor conditions may not benefit from this research.

What this research studies

This research investigates the genetic events that differentiate benign conditions from malignant multiple myeloma precursor stages. By utilizing advanced whole genome sequencing, the study aims to identify critical genomic markers that indicate whether a patient’s condition is stable or likely to progress to multiple myeloma. The goal is to enable early identification of high-risk patients, allowing for timely intervention and prevention strategies. This approach could significantly improve patient outcomes by addressing a major unmet clinical need in the management of myeloma precursor conditions.

Why it matters

Potential benefit: If successful, this research could lead to earlier diagnosis and prevention strategies for patients at risk of developing multiple myeloma.

How similar studies have gone: Previous research has shown success in using whole genome sequencing to identify genomic events in various cancers, suggesting that this approach may be effective in the context of myeloma precursor conditions as well.

Where this research is happening

  • University of Miami School of Medicine
    Coral Gables, United States
    Active

Researchers

  • Principal investigator: Maura, Francesco — University of Miami School of Medicine
  • Study coordinator: Maura, Francesco

Related research

Other NIH-funded projects on the same topics.

About this research

  1. This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
  2. Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
  3. For full project details, budget, and progress reports, visit the official NIH RePORTER page.
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.